A truncating mutation in B3GNT1 causes severe Walker–Warburg syndrome

Author: Shaheen Ranad   Faqeih Eissa   Ansari Shinu   Alkuraya Fowzan  

Publisher: Springer Publishing Company

ISSN: 1364-6745

Source: Neurogenetics, Vol.14, Iss.3-4, 2013-11, pp. : 243-245

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