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A homozygous female hemophilia A

BACKGROUND: Hemophilia A (HA), being an X-linked recessive disorder, females are rarely affected, although they can be carriers. AIMS: To study the mutation in F8 gene in an extended family with a homozygous female HA. MATERIALS AND METHODS: All the seven affected members (six males and one female)...

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Hlavní autoři: Nair, Preethi S., Shetty, S., Ghosh, Kanjaksha
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2012
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3385172/
https://ncbi.nlm.nih.gov/pubmed/22754241
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.96685
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