Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Miguel Villegas-Aguilera"'
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 73, Iss 3, Pp 196-201 (2016)
Introducción: La enfermedad de Alexander consiste en una forma de leucodistrofia poco frecuente que afecta principalmente a los astrocitos; tiene un patrón de herencia autosómica recesiva y es causada por mutaciones en el gen GFAP, localizado en e
Externí odkaz:
https://doaj.org/article/879a2894a3844fc4b1e4a661749e74cf
Autor:
Miguel Villegas-Aguilera, Héctor Gerardo Hernández-Rodríguez, Antonio Bravo-Oro, Claudia Lizbeth Gómez-Elías, Rosalina Rivera-Vega, Luís Fernando Mendoza-Moreno, Jorge Guillermo Reyes-Vaca, Jorge Luís García-Ramírez
Publikováno v:
Revista Mexicana de Neurociencia. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2096f2f7544118af46240d33332b9bb5
https://doi.org/10.24875/rmn.m18000012
https://doi.org/10.24875/rmn.m18000012
Publikováno v:
Boletín Médico Del Hospital Infantil de México (English Edition). 73:196-201
Background Alexander disease is a rare form of leukodystrophy that involves mainly astrocytes; it is inherited in an autosomal recessive manner and occurs by mutations in the GFAP gene, located on chromosome 17q21. It can occur at any age, and its in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e0d8199ef9bc7ecf3407e24fad7e1fa
https://doi.org/10.1016/j.bmhime.2017.08.002
https://doi.org/10.1016/j.bmhime.2017.08.002
Publikováno v:
Boletin medico del Hospital Infantil de Mexico. 73(3)
Alexander disease is a rare form of leukodystrophy that involves mainly astrocytes; it is inherited in an autosomal recessive manner and occurs by mutations in the GFAP gene, located on chromosome 17q21. It can occur at any age and its infantile form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7d11cb557569f497f39fbff719e71a98
https://pubmed.ncbi.nlm.nih.gov/29421207
https://pubmed.ncbi.nlm.nih.gov/29421207