Javad Karimian

Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems

F. Hadipour, Z. Hadipour, F. Behjati, 2020, Molecular Syndromology.

Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability.

F. Behjati, Vahid Asghariazar, Ahoura Nozari, 2020, Gene.