A clinical review of Charcot-Marie-Tooth (Q33787301)

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Language	Label	Description	Also known as
English	A clinical review of Charcot-Marie-Tooth	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

review article

1 reference

stated in

Europe PubMed Central

title

A clinical review of Charcot-Marie-Tooth (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

author name string

Garcia CA

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

published in

Annals of the New York Academy of Sciences

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

volume

883

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

page(s)

69-76

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

cites work

Hereditary motor-sensory neuropathy and movement disorders

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08570.X

retrieved

21 January 2018

A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08570.X

retrieved

21 January 2018

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08570.X

retrieved

21 January 2018

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08570.X

retrieved

21 January 2018

Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08570.X

retrieved

21 January 2018

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08570.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1749-6632.1999.TB08570.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

PubMed publication ID

10586233

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10586233

retrieved

29 July 2017

29086999

reason for deprecated rank

unchecked identifier

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