Identification of rare copy number variations reveals PJA2 , APCS , SYNPO , and TAC1 as novel candidate genes in Autism Spectrum Disorders-Reference-Cited by-同舟云学术

Identification of rare copy number variations reveals PJA2 , APCS , SYNPO , and TAC1 as novel candidate genes in Autism Spectrum Disorders

Published:2019-06-29 Issue:8 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Bitar Tania¹²^ORCID,Hleihel Walid²^ORCID,Marouillat Sylviane¹,Vonwill Sandrine¹³,Vuillaume Marie‐Laure¹³^ORCID,Soufia Michel⁴,Vourc'h Patrick¹³,Laumonnier Frederic¹,Andres Christian R.¹³^ORCID

Affiliation:

1. INSERM U1253 ibrain Université de Tours Tours France

2. Faculty of Sciences Holy Spirit University of Kaslik (USEK) Jounieh Lebanon

3. CHRU de Tours Tours France

4. Faculty of Medicine Holy spirit University of Kaslik (USEK) Jounieh Lebanon

Funder

Conseil National de la Recherche Scientifique au Liban

Higher Center for Research - Holy Spirit University of Kaslik

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.786

Reference24 articles.

1. A girl with developmental delay, ataxia, cranial nerve palsies, severe respiratory problems in infancy-Expanding NDST1 syndrome

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4. Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: The case of synapsins;Giovedí S.;Frontiers in Pediatrics,2014

5. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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