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Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg–Hirschsprung disease: Phenotypes linked by SOX10 mutation

✍ Scribed by Ken Inoue; Konstantin Shilo; Cornelius F. Boerkoel; Carol Crowe; Joram Sawady; James R. Lupski; Dimitri P. Agamanolis


Book ID
101464162
Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
202 KB
Volume
52
Category
Article
ISSN
0364-5134

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