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PubMed (GeneRIF) for id: 55907
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A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family.
Ann Hum Genet. 2020 Jan;84(1):46-53. doi: 10.1111/ahg.12349. Epub 2019 Sep 8.
Ann Hum Genet. 2020.
PMID: 31495922
CMP‑N‑acetylneuraminic acid synthetase interacts with fragile X related protein 1.
Ma Y, Tian S, Wang Z, Wang C, Chen X, Li W, Yang Y, He S.
Ma Y, et al.
Mol Med Rep. 2016 Aug;14(2):1501-8. doi: 10.3892/mmr.2016.5438. Epub 2016 Jun 23.
Mol Med Rep. 2016.
PMID: 27357083
Free PMC article.
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