(Q51917663)
Statements
A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype (English)
Wolfram Heinritz
Ursula G Froster
Sibylle Strenge
Annegret Kujat
Steffen Syrbe
Volker Schuster
scientific article published in June 2006