GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms-Reference-Cited by-同舟云学术

GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms

Published:2020-12-02 Issue:2 Volume:185 Page:476-485
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Mademont‐Soler Irene¹^ORCID,Casellas‐Vidal Dolors²^ORCID,Trujillo Alberto²,Espuña‐Capote Núria²,Maroto Anna³,García‐González Maria del Mar²,Ruiz María Dolores⁴,Diego‐Álvarez Dan⁴,Queralt Xavier¹,Perapoch Josep²,Obón María¹

Affiliation:

1. Àrea de Genètica Clínica i Consell Genètic Laboratori Clínic Territorial Girona, Institut Català de la Salut Girona Spain

2. Servei de Pediatria Hospital Universitari Doctor Josep Trueta Girona Spain

3. Servei de Ginecologia i Obstetrícia Hospital Universitari Doctor Josep Trueta Girona Spain

4. Unidad Citogenómica Sistemas Genómicos Paterna Spain

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61996

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5. The specification of Glycinergic neurons and the role of Glycinergic transmission in development;Chalphin A. V.;Frontiers in Molecular Neuroscience,2010

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