Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphatemic familial tumoral calcinosis

Normophosphatemic familial tumoral calcinosis, characterized by ectopic mineralization of skin, is caused by mutations in the SAMD9 gene located on human chromosome 7q21, next to a paralogous gene, SAMD9-like (SAMD9L). Mouse does not have a SAMD9 orthologue, Samd9, because it has been deleted during...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Li, Qiaoli, Guo, Haitao, Matsui, Hirotaka, Honda, Hiroaki, Inaba, Toshiya, Sundberg, John P., Sprecher, Eli, Uitto, Jouni
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2012
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3381902/
https://ncbi.nlm.nih.gov/pubmed/22716256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1600-0625.2012.01524.x
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