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HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRI

✍ Scribed by Kaan Boztug; Xiao-Qi Ding; Hans Hartmann; Lena Ziesenitz; Alejandro A. Schäffer; Jana Diestelhorst; Dietmar Pfeifer; Giridharan Appaswamy; Sonja Kehbel; Thorsten Simon; Abdullah Al Jefri; Heinrich Lanfermann; Christoph Klein


Book ID
101451769
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
320 KB
Volume
152A
Category
Article
ISSN
1552-4825

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