A Novel Mutation in RPL10(Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia
HUMAN MUTATION (2015)
期刊
HUMAN MUTATION
卷 36, 期 12, 页码 1155-1158出版社
WILEY-BLACKWELL
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资金
- Italian Telethon [GGP08145]
- Italian Ministry of Health (RF)
- German Ministry of Education and Research through the MRNET
- EU [241995]
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