NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

Author:

Al Shehhi Maryam,Forman Eva B.,Fitzgerald Jacqueline E.,McInerney Veronica,Krawczyk Janusz,Shen Sanbing,Betts David R.,Ardle Linda Mc,Gorman Kathleen M.,King Mary D.,Green Andrew,Gallagher LouiseORCID,Lynch Sally A.ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference18 articles.

1. Beta-neurexins control neural circuits by regulating synaptic endocannabinoid signaling;Anderson;Cell,2015

2. Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature;Bena;Am. J. Med. Genet. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics,2013

3. Evidence for the multiple hits genetic theory for inherited language impairment: a case study;Centanni;Front. Genet.,2015

4. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders;Ching;Am. J. Med. Genet. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics,2010

5. Investigation of NRXN1 deletions: clinical and molecular characterization;Dabell;Am. J. Med. Genet.,2013

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