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Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.
Am J Hum Genet. 2012 Feb 10;90(2):356-62. doi: 10.1016/j.ajhg.2011.12.018. Epub 2012 Jan 26.
Am J Hum Genet. 2012.
PMID: 22284827
Free PMC article.
A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family.
Hazan F, Ostergaard P, Ozturk T, Kantekin E, Atlihan F, Jeffery S, Ozkinay F.
Hazan F, et al.
Am J Med Genet A. 2012 Jul;158A(7):1686-9. doi: 10.1002/ajmg.a.35371. Epub 2012 May 31.
Am J Med Genet A. 2012.
PMID: 22653704
Free article.
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