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Heterozygous FA2H mutations in autism spectrum disorders.
Scheid I, Maruani A, Huguet G, Leblond CS, Nygren G, Anckarsäter H, Beggiato A, Rastam M, Amsellem F, Gillberg IC, Elmaleh M, Leboyer M, Gillberg C, Betancur C, Coleman M, Hama H, Cook EH, Bourgeron T, Delorme R. Scheid I, et al. Among authors: hama h. BMC Med Genet. 2013 Dec 3;14:124. doi: 10.1186/1471-2350-14-124. BMC Med Genet. 2013. PMID: 24299421 Free PMC article.
The human FA2H gene encodes a fatty acid 2-hydroxylase.
Alderson NL, Rembiesa BM, Walla MD, Bielawska A, Bielawski J, Hama H. Alderson NL, et al. Among authors: hama h. J Biol Chem. 2004 Nov 19;279(47):48562-8. doi: 10.1074/jbc.M406649200. Epub 2004 Aug 27. J Biol Chem. 2004. PMID: 15337768 Free article.
246 results