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“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

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