A developmental and genetic classification for midbrain-hindbrain malformations
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/132/12/3199/1318842/awp247.pdf
Reference320 articles.
1. Aicardi syndrome
2. Mutations of the POMT1 gene found in patients with Walker–Warburg syndrome lead to a defect of protein O-mannosylation
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