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Variable clinical expression of an identical mutation in the ATP7A gene for Menkes disease/Occipital horn syndrome in three affected males in a single family

✍ Scribed by Bettina Borm; Lisbeth Birk Møller; Ingrid Hausser; Michael Emeis; Kurt Baerlocher; Nina Horn; Rainer Rossi


Book ID
116682743
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
584 KB
Volume
145
Category
Article
ISSN
1097-6833

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