(Q36780889)

16 August 2017

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title

Autosomal-recessive and X-linked forms of hereditary motor and sensory neuropathy in childhood (English)

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hereditary motor and sensory neuropathy

16 August 2017

main subject

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Monique M Ryan

3

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author name string

Robert Ouvrier

series ordinal

1

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16 August 2017

Nimeshan Geevasingha

series ordinal

2

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16 August 2017

publication date

1 August 2007

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16 August 2017

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16 August 2017

volume

36

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16 August 2017

issue

2

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16 August 2017

page(s)

131-143

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SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma

16 August 2017

cites work

1 reference

Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene.

21 January 2018

1 reference

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.

21 January 2018

1 reference

Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype

21 January 2018

1 reference

Autosomal-recessive Charcot-Marie-Tooth diseases

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.20776

1 reference

16 August 2017

1 reference