Open AccessWhole exome sequencing reveals complex inheritance patterns and identifies two gene mutations implicated in the development of Autism and Intellectual Disability in a consanguineous Palestinian family
Author(s) -
Reham KhalafNazzal,
Imad Dweikat,
Maqboul Arwa
Publication year - 2016
Publication title -
frontiers in neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.499
H-Index - 102
eISSN - 1662-4548
pISSN - 1662-453X
DOI - 10.3389/conf.fnins.2016.92.00010
Subject(s) - exome sequencing , autism , intellectual disability , consanguinity , genetics , medicine , autism spectrum disorder , exome , phenotype , biology , gene , psychiatry