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pro vyhledávání: '"Lori Beth Swenson"'
Autor:
Hua Li, Heinz Arnheiter, Lori Beth Swenson, Atsuo Nakayama, Colin A. Hodgkinson, Thomas M Glaser, Karin Opdecamp, James H. Asher
Publikováno v:
Human molecular genetics. 7(4)
Mutations in MITF (microphthalmia transcription factor) cause Waardenburg syndrome type 2 (WS2A) in humans, an autosomal dominant disorder consisting of deafness and hypopigmentation. Phenotypes vary significantly within WS2 pedigrees, and there is g