“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”

Detalles Bibliográficos
Autores principales: Arowolo, Afolake T., Adeola, Henry A., Khumalo, Nonhlanhla P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747945/
https://www.ncbi.nlm.nih.gov/pubmed/29287597
http://dx.doi.org/10.1186/s12969-017-0215-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747945/
https://www.ncbi.nlm.nih.gov/pubmed/29287597
http://dx.doi.org/10.1186/s12969-017-0215-8

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