Report of a family affected with autism and non syndromic intellectual disability caused by a mutation in PTCHD1, an X-linked gene coding for a transmembrane protein expressed in postsynaptic dendritic spines

Cottereau, E; Papon, M-A; Marouillat, S; Antar, C; Chelly, J; Van Bokhoven, H; Van Esch, Hilde; Raynaud, M; Ropers, H-H; Andres, C; Laumonnier, F; toutain, A

Genetic Counseling

Report of a family affected with autism and non syndromic intellectual disability caused by a mutation in PTCHD1, an X-linked gene coding for a transmembrane protein expressed in postsynaptic dendritic spines

Author:

Cottereau, E

Papon, M-A ; Marouillat, S ; Antar, C ; Chelly, J ; Van Bokhoven, H ; Van Esch, Hilde ; Raynaud, M ; Ropers, H-H ; Andres, C ; Laumonnier, F ; toutain, A

Keywords:

2203 Philosophy, Genetics & Heredity, 5001 Applied ethics

Genetic Counseling Report of a family affected with autism and non syndromic intellectual disability caused by a mutation in PTCHD1, an X-linked gene coding for a transmembrane protein expressed in postsynaptic dendritic spines

Author:

Keywords:

Genetic Counseling

Report of a family affected with autism and non syndromic intellectual disability caused by a mutation in PTCHD1, an X-linked gene coding for a transmembrane protein expressed in postsynaptic dendritic spines