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Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients
BACKGROUND: Hemophilia A (HA) is an inherited X‐linked recessive coagulation disorder caused by factor VIII (F8) deficiency. F8 rearrangements involving intron 22 (int22) and intron 1 (int1) account for almost half of severe HA phenotype also a hotspot exon 14 provides numerous mutational patterns....
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8077131/ https://ncbi.nlm.nih.gov/pubmed/33342086 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1575 |
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