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Keutel Syndrome, a Review of 50 Years of Literature
Keutel syndrome (KS) is a rare autosomal recessive genetic disorder that was first identified in the beginning of the 1970s and nearly 30 years later attributed to loss-of-function mutations in the gene coding for the matrix Gla protein (MGP). Patients with KS are usually diagnosed during childhood...
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| Publicado no: | Front Cell Dev Biol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8117146/ https://ncbi.nlm.nih.gov/pubmed/33996798 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2021.642136 |
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