New insights into the metabolic and nutritional determinants of severe combined immunodeficiency

Human mutations in MTHFD1 have recently been identified in patients with severe combined immunodeficiency (SCID). SCID results from inborn errors of metabolism that cause impaired T- and B-cell proliferation and function. One of the most common causes of SCID is adenosine deaminase (ADA) deficiency,...

Descripción completa

Detalles Bibliográficos
Autores principales: Field, Martha S, Kamynina, Elena, Watkins, David, Rosenblatt, David S, Stover, Patrick J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817835/
https://www.ncbi.nlm.nih.gov/pubmed/27123375
http://dx.doi.org/10.1080/21675511.2015.1112479

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817835/
https://www.ncbi.nlm.nih.gov/pubmed/27123375
http://dx.doi.org/10.1080/21675511.2015.1112479

Ejemplares similares