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Prenatal genetic testing for familial severe congenital protein C deficiency
Severe congenital protein C (PC) deficiency is an autosomal recessive hereditary thrombophilia caused by mutations in PROC. The case manifested severe purpura fulminans, intracranial thrombosis or hemorrhage within 4 days after birth, resulting in blindness. We report the identification of inherited...
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| Publicado no: | Hum Genome Var |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4785544/ https://ncbi.nlm.nih.gov/pubmed/27081530 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2015.17 |
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