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Quoted phrase not found in phrase index: "Warburg micro syndrome 3"
Page 1
Novel RAB3GAP1 compound heterozygous mutations in Japanese siblings with Warburg Micro syndrome.
Brain Dev. 2016 Mar;38(3):337-40. doi: 10.1016/j.braindev.2015.09.006. Epub 2015 Oct 1.
Brain Dev. 2016.
PMID: 26421802
BACKGROUND: Warburg Micro syndrome (WARBM) is a rare autosomal recessive disease characterized by postnatal growth retardation, microcephaly, severely delayed motor and intellectual development, microcornea, congenital cataracts, optic atrophy, and hypogonadi …
BACKGROUND: Warburg Micro syndrome (WARBM) is a rare autosomal recessive disease characterized by postnatal growth reta …
Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice.
Park AK, Liegel RP, Ronchetti A, Ebert AD, Geurts A, Sidjanin DJ.
Park AK, et al.
BMC Genet. 2014 Dec 5;15:135. doi: 10.1186/s12863-014-0135-2.
BMC Genet. 2014.
PMID: 25476608
Free PMC article.
BACKGROUND: Loss-of-function mutations in TBC1D20 cause Warburg Micro syndrome 4 (WARBM4), which is an autosomal recessive syndromic disorder characterized by eye, brain, and genital abnormalities. Blind sterile (bs) mice carry a Tbc1d20-null mutation and exh …
BACKGROUND: Loss-of-function mutations in TBC1D20 cause Warburg Micro syndrome 4 (WARBM4), which is an autosomal recess …
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