De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability
Titel:
De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability
Auteur:
Grozeva, Detelina Carss, Keren Spasic-Boskovic, Olivera Parker, Michael J. Archer, Hayley Firth, Helen V. Park, Soo-Mi Canham, Natalie Holder, Susan E. Wilson, Meredith Hackett, Anna Field, Michael Floyd, James A.B. Hurles, Matthew Raymond, F. Lucy