Commentary: New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2

Detalles Bibliográficos
Autor principal: Finsterer, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598496/
https://www.ncbi.nlm.nih.gov/pubmed/31293567
http://dx.doi.org/10.3389/fimmu.2019.01333

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598496/
https://www.ncbi.nlm.nih.gov/pubmed/31293567
http://dx.doi.org/10.3389/fimmu.2019.01333

Ejemplares similares