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Details on Person A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease
| Class:Id | LiteratureReference:9619264 |
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| _displayName | A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease |
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| _timestamp | 2018-09-14 19:09:24 |
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| author | [Person:9619266] Guilbot, Angèle
[Person:9619260] Williams, Anna
[Person:9619265] Ravisé, Nicole
[Person:9619262] Verny, Christophe
[Person:5602247] Brice, Alexis
[Person:9619267] Sherman, Diane L
[Person:9619268] Brophy, Peter J
[Person:9619261] LeGuern, Eric
[Person:9619258] Delague, Valérie
[Person:9619263] Bareil, Corinne
[Person:2730971] Megarbane, André
[Person:9619269] Claustres, Mireille |
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| created | [InstanceEdit:9619259] Rothfels, Karen, 2018-09-14 |
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| journal | Hum. Mol. Genet. |
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| pages | 415-21 |
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| pubMedIdentifier | 11157804 |
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| title | A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease |
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| volume | 10 |
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| year | 2001 |
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| (literatureReference) | [Reaction:9619657] EGR2 and SOX10 bind the PRX gene [Homo sapiens]
[BlackBoxEvent:9619667] PRX gene expression [Homo sapiens] |
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