Molecular Genetics of Charcot-Marie-Tooth Neuropathy

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Myelin mutants: model systems for the study of normal and abnormal myelination.Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene

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Molecular Genetics of Charcot-Marie-Tooth Neuropathy

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http://www.wikidata.org/entity/Q55919481

description

article

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wetenschappelijk artikel

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наукова стаття, опублікована в 1994

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ലേഖനം

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name

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

@en

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

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type

Item

label

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

@en

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

@nl

prefLabel

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

@en

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

@nl

P1476

Molecular Genetics of Charcot-Marie-Tooth Neuropathy

@en

P2093

Benjamin B. Roa

http://www.w3.org/2001/XMLSchema#string

James R. Lupski

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P304

117-152

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P31

scholarly article

P356

10.1007/978-1-4757-9062-7_3

http://www.w3.org/2001/XMLSchema#string

P577

1994-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime