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“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
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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