Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7 (Q34388920)

1 August 2017

title

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7 (English)

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autosomal dominant limb-girdle muscular dystrophy

1 August 2017

main subject

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author

Margaret A. Pericak-Vance

12

object named as

M A Pericak-Vance

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1 August 2017

M C Speer

1

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1 August 2017

J M Vance

2

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1 August 2017

J M Grubber

3

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1 August 2017

F Lennon Graham

4

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1 August 2017

J M Stajich

5

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1 August 2017

K D Viles

6

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1 August 2017

A Rogala

7

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1 August 2017

R McMichael

8

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1 August 2017

J Chutkow

9

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1 August 2017

C Goldsmith

10

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1 August 2017

R W Tim

11

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1 August 2017

language of work or name

English

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publication date

1 February 1999

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

64

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1 August 2017

issue

2

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1 August 2017

page(s)

556-562

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Formal genetics of muscular dystrophy

1 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Caveolin-3 in muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

A population study of adult onset limb-girdle muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Adult-onset autosomal dominant limb-girdle muscular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Estimating the power of a proposed linkage study: a practical computer simulation approach

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Computer programs for multilocus haplotyping of general pedigrees.

6 July 2018

1 reference

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Genetic studies of a family with two unusual autosomal dominant conditions: muscular dystrophy and Pelger-Huet anomaly. Clinical, pathologic and linkage considerations

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377765

Autosomal recessive muscular dystrophy in Manitoba Hutterites*

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9973293

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9973293

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/302252

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1 August 2017

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1 August 2017

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