TY  - GEN
AU  - Lahbib,Saida
AU  - Leblond,Claire S
AU  - Hamza,Mariem
AU  - Regnault,Béatrice
AU  - Lemée,Laure
AU  - Mathieu,Alexandre
AU  - Jaouadi,Hager
AU  - Mkaouar,Rahma
AU  - Youssef-Turki,Ilhem Ben
AU  - Belhadj,Ahlem
AU  - Kraoua,Ichraf
AU  - Bourgeron,Thomas
AU  - Abdelhak,Sonia
TI  - Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
SN  - 2190-3883
PY  - 2019///0516
KW  - Adolescent
KW  - Autism Spectrum Disorder
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 2
KW  - Female
KW  - GTPase-Activating Proteins
KW  - Hearing Loss
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Male
KW  - Pedigree
KW  - Sequence Deletion
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/s13353-018-0472-3
ER  -