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To the Editor : Mutations in the faciogenital dysplasia 1 (FGD1 ) gene are responsible for Aarskog-Scott syndrome (AAS; OMIM #305400), a rare X-linked disorder characterized by typical facial features, as well as skeletal and genital anomalies (1). The 18 coding exons of the FGD1 gene encode a guanine nucleotide exchange factor (GEF) which specifically(More)
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