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Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion

✍ Scribed by Nicol C. Voermans; Tjitske Kleefstra; Anneke A. Gabreëls-Festen; Brigitte H. W. Faas; Erik-Jan Kamsteeg; Henry Houlden; Matilde Laurá; James M. Polke; Amelie Pandraud; Fred van Ruissen; Baziel G. van Engelen; Mary M. Reilly


Book ID
114748466
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
462 KB
Volume
17
Category
Article
ISSN
1085-9489

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