Evaluation of factor VIII polymorphic short tandem repeat markers in linkage analysis for carrier diagnosis of hemophilia A

Hemophilia A (HA) is the most common inherited X-linked recessive bleeding disorder caused by heterogeneous mutations in the factor VIII gene (FVIII). Diagnosis of the carrier is critical for preventing the birth of children affected by this coagulation disorder, which ultimately facilitates its man...

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Udgivet i:Biomed Rep
Main Authors: Shrestha, Sabina, Dong, Sufang, Li, Zuhua, Huang, Zhuliang, Zheng, Fang
Format: Artigo
Sprog:Inglês
Udgivet: D.A. Spandidos 2016
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4950737/
https://ncbi.nlm.nih.gov/pubmed/27446547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/br.2016.712
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