Novel EGR2 variant that associates with Charcot-Marie-Tooth disease when combined with lipopolysaccharide-induced TNF-a factor T49M polymorphism

Autor:	Blanco-Cantó ME, Patel N, Velasco-Aviles S, Casillas-Bajo A, Salas-Felipe J, García-Escrivá A, Díaz-Marín C, Cabedo H
Rok vydání:	2020
Předmět:	musculoskeletal diseases stomatognathic diseases congenital hereditary and neonatal diseases and abnormalities stomatognathic system nervous system diseases
Zdroj:	NEUROLOGY-GENETICS r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante instname
ISSN:	2376-7839
Popis:	To identify novel genetic mechanisms causing Charcot-Marie-Tooth (CMT) disease.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::ded3dd4739c3a7397cad6a81a2032d7f https://fundanet.isabial.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=5877 Zobrazit plný text záznamu