Unilateral focal polymicrogyria in a patient with classical Aarskog–Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1
Armand Bottani, Alfredo Orrico, Lucia Galli, Olivier Karam, Charles-André Haenggeli, Solène Ferey, Bernard ConradVolume:
143A
Year:
2007
Language:
english
Pages:
5
DOI:
10.1002/ajmg.a.31733
File:
PDF, 224 KB
english, 2007