TY  - GEN
AU  - Torrico,Bàrbara
AU  - Fernàndez-Castillo,Noèlia
AU  - Hervás,Amaia
AU  - Milà,Montserrat
AU  - Salgado,Marta
AU  - Rueda,Isabel
AU  - Buitelaar,Jan K
AU  - Rommelse,Nanda
AU  - Oerlemans,Anoek M
AU  - Bralten,Janita
AU  - Freitag,Christine M
AU  - Reif,Andreas
AU  - Battaglia,Agatino
AU  - Mazzone,Luigi
AU  - Maestrini,Elena
AU  - Cormand,Bru
AU  - Toma,Claudio
TI  - Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability
SN  - 1476-5438
PY  - 2016///0824
KW  - Autism Spectrum Disorder
KW  - genetics
KW  - Case-Control Studies
KW  - Cell Line, Tumor
KW  - Female
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Membrane Proteins
KW  - Mutation, Missense
KW  - Polymorphism, Single Nucleotide
KW  - Promoter Regions, Genetic
KW  - Trinucleotide Repeats
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ejhg.2015.37
ER  -