![](/img/cover-not-exists.png)
HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRI
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 LanVolume:
152A
Year:
2010
Language:
english
Pages:
7
DOI:
10.1002/ajmg.a.33748
File:
PDF, 320 KB
english, 2010