Human Genome Epidemiology Literature Finder

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Query Trace: Disease and PAFAH1B1[original query]
Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification. Brain & development 2018 8 41 (1): 29-35. Shi Chang-He, Zhang Shuo, Yang Zhi-Hua, Liu Yu-Tao, Li Yu-Sheng, Li Zhuo, Hu Zheng-Wei, Xu Yu-Mi Similar articles in PubMed