Additional file 1: of Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy
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https://springernature.figshare.com/articles/Additional_file_1_of_Recessive_mutations_in_ATP8A2_cause_severe_hypotonia_cognitive_impairment_hyperkinetic_movement_disorders_and_progressive_optic_atrophy/6823811/1
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资源简介：
Table S1. Exome sequencing of individuals with ATP8A2 mutations. (XLSX 11 kb)
提供机构：
Mohammadreza Dehghani; Islay Thompson
创建时间：
2018-07-17
