Published in
Springer (part of Springer Nature), Journal of Applied Genetics, 1(60), p. 49-56, 2018
DOI: 10.1007/s13353-018-0472-3
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Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
Journal article published in 2018 by
Saida Lahbib 
,
Claire S. Leblond,
Mariem Hamza,
Béatrice Regnault ,
Laure Lemée,
Alexandre Mathieu,
Hager Jaouadi,
Rahma Mkaouar,
Ilhem Ben Youssef-Turki,
Ahlem Belhadj,
Ichraf Kraoua,
Thomas Bourgeron,
Sonia Abdelhak
,
Claire S. Leblond,
Mariem Hamza,
Béatrice Regnault ,
Laure Lemée,
Alexandre Mathieu,
Hager Jaouadi,
Rahma Mkaouar,
Ilhem Ben Youssef-Turki,
Ahlem Belhadj,
Ichraf Kraoua,
Thomas Bourgeron,
Sonia Abdelhak
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