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Literature for OMIM 248200: STARGARDT DISEASE 1; STGD1
Xenbase Articles:
( Denotes literature images)
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies., Wiszniewski W,Yatsenko AN,Jamrich M,Wensel TG,Lewis RA,Lupski JR,Zaremba CM, Hum Mol Genet. October 1, 2005; 14(19):1460-2083. |