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Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by the complete absence of detectable fibrinogen. Uncontrolled bleeding after birth from the umbilical cord is common, and spontaneous intracerebral bleeding and splenic rupture can occur throughout life. Patients respon...
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| Publicado no: | J Clin Invest |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
1999
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC407887/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9916133/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI5471 |
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