RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing.

Albury, Cassie L; Gerring, Zachary F; Griffiths, Lyn R; Nyholt, Dale R; Rodriguez-Acevedo, Astrid J

Albury, Cassie L; Gerring, Zachary F; Griffiths, Lyn R; Nyholt, Dale R; Rodriguez-Acevedo, Astrid J.

Afiliação

Albury CL; a Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane , Australia.
Gerring ZF; b Statistical and Genomic Epidemiology Laboratory , Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane , Australia.
Griffiths LR; a Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane , Australia.
Nyholt DR; b Statistical and Genomic Epidemiology Laboratory , Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane , Australia.
Rodriguez-Acevedo AJ; c Xavier University School of Medicine , Oranjestad , Aruba.

J Neurogenet ; 31(4): 320-321, 2017 12.

Article em En | MEDLINE | ID: mdl-29105529

Assuntos

Epilepsia/genética; Enxaqueca sem Aura/genética; Exoma; Predisposição Genética para Doença; Humanos; Mutação de Sentido Incorreto

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Enxaqueca sem Aura / Epilepsia Limite: Humans Idioma: En Revista: J Neurogenet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google