Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology

• Autorzy: Lahbib S. , Leblond C.S. , Hamza M. , Regnault B. , Lemee L. , Mathieu A. , Jaouadi H. , Mkaouar R. , Youssef-Turki I.B. , Belhadj A. , Kraoua I. , Bourgeron T. , Abdelhak S.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2019
• Tom: 60
• Numer: 1
• Opis fizyczny: p.49-56,fig.,ref.

Twórcy

autor

Lahbib S.

• Biomedical Genomics and Oncogenetics Laboratory LR16IPT05, Universite Tunis El Manar, Institut Pasteur de Tunis, 1002, Tunis, Tunisia
• University of Tunis El Manar, Tunis, Tunisia

autor

Leblond C.S.

• Human Genetics and Cognitive Functions Unit, Institut Pasteur, 75015, Paris, France
• CNRS UMR3571, Genes, Synapses and Cognition, Institut Pasteur, 75015, Paris, France
• Paris Diderot University, Sorbonne Paris Cite, 75013, Paris, France

autor

Hamza M.

• Faculty of Medicine of Tunis, University of Tunis El Manar, 1007 La Rabta, Tunis, Tunisia
• Child and Adolescent Psychiatry Department, Mongi Slim Hospital, 2046, Sidi Daoud, Tunisia

autor

Regnault B.

• Plateforme de Genotypage des Eucaryotes, Centre d'Innovation et Recherche Technologique (CITECH), Institut Pasteur, 75015, Paris, France

autor

Lemee L.

• Plateforme de Genotypage des Eucaryotes, Centre d'Innovation et Recherche Technologique (CITECH), Institut Pasteur, 75015, Paris, France

autor

Mathieu A.

• Human Genetics and Cognitive Functions Unit, Institut Pasteur, 75015, Paris, France
• CNRS UMR3571, Genes, Synapses and Cognition, Institut Pasteur, 75015, Paris, France
• Paris Diderot University, Sorbonne Paris Cite, 75013, Paris, France

autor

Jaouadi H.

• Biomedical Genomics and Oncogenetics Laboratory LR16IPT05, Universite Tunis El Manar, Institut Pasteur de Tunis, 1002, Tunis, Tunisia

autor

Mkaouar R.

• Biomedical Genomics and Oncogenetics Laboratory LR16IPT05, Universite Tunis El Manar, Institut Pasteur de Tunis, 1002, Tunis, Tunisia

autor

Youssef-Turki I.B.

• Faculty of Medicine of Tunis, University of Tunis El Manar, 1007 La Rabta, Tunis, Tunisia
• Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, 1007, Tunis, Tunisia

autor

Belhadj A.

• Faculty of Medicine of Tunis, University of Tunis El Manar, 1007 La Rabta, Tunis, Tunisia
• Child and Adolescent Psychiatry Department, Mongi Slim Hospital, 2046, Sidi Daoud, Tunisia

autor

Kraoua I.

• Faculty of Medicine of Tunis, University of Tunis El Manar, 1007 La Rabta, Tunis, Tunisia
• Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, 1007, Tunis, Tunisia

autor

Bourgeron T.

• Human Genetics and Cognitive Functions Unit, Institut Pasteur, 75015, Paris, France
• CNRS UMR3571, Genes, Synapses and Cognition, Institut Pasteur, 75015, Paris, France
• Paris Diderot University, Sorbonne Paris Cite, 75013, Paris, France

autor

Abdelhak S.

• Biomedical Genomics and Oncogenetics Laboratory LR16IPT05, Universite Tunis El Manar, Institut Pasteur de Tunis, 1002, Tunis, Tunisia

Identyfikatory

DOI

10.1007/s13353-018-0472-3