Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene

Detalles Bibliográficos
Autores principales: Hasegawa, Kosei, Higuchi, Yosuke, Yamashita, Miho, Tanaka, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2015
Materias:
Mutation-in-Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322291/
https://www.ncbi.nlm.nih.gov/pubmed/25678758
http://dx.doi.org/10.1297/cpe.24.33

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322291/
https://www.ncbi.nlm.nih.gov/pubmed/25678758
http://dx.doi.org/10.1297/cpe.24.33

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