A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)

Autor: Orrico, A., Galli, L., Falciani, M., Bracci, M., Cavaliere, M. L., Rinaldi, M. M., Musacchio, A., Sorrentino, V.
Zdroj: FEBS Letters; 2000, Vol. 478 Issue: 3 p216-220, 5p
Databáze: Supplemental Index