An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy (Q24320265)

congenital muscular dystrophy

GOA release 2020-03-11

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K Kobayashi

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Y Nakahori

2

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M Miyake

3

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K Matsumura

4

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E Kondo-Iida

5

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Y Nomura

6

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M Segawa

7

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M Yoshioka

8

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K Saito

9

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M Osawa

10

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K Hamano

11

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Y Sakakihara

12

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I Nonaka

13

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Y Nakagome

14

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I Kanazawa

15

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Y Nakamura

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K Tokunaga

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T Toda

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

18

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language of work or name

English

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publication date

23 July 1998

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published in

Nature

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volume

394

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issue

6691

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page(s)

388-92

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cites work

1 reference

Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).

21 January 2018

1 reference

YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.

21 January 2018

1 reference

A knowledge base for predicting protein localization sites in eukaryotic cells

21 January 2018

1 reference

Messenger RNA degradation in eukaryotes

21 January 2018

1 reference

Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

1 reference

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

21 January 2018

1 reference

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex

21 January 2018

1 reference

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

Abnormal localization of laminin subunits in muscular dystrophies

21 January 2018

1 reference

Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? Pathological study of the cerebral cortex of an FCMD fetus

21 January 2018

1 reference

Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

21 January 2018

1 reference

21 January 2018

1 reference

Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice

21 January 2018

1 reference

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

1 reference

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

21 January 2018

1 reference

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

21 January 2018

1 reference

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Discrimination of human HLA-DRB1 alleles by PCR-SSCP (single-strand conformation polymorphism) method

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

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Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1018554032

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1046686728

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1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

9690476

1 reference

Consolidated OpenCitations Corpus – April 2017