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HindIII-based restriction fragment length polymorphism in hemophilic and nonhemophilic patients
Hemophilia A is most common recessively inherited bleeding disorder, which affect one in five thousand male births throughout the world. In most of the hemophilic A patients, no common mutation is easily identifiable. This limitation has been overcome by the use of polymorphic DNA marker, i.e., rest...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications Pvt Ltd
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3217284/ https://ncbi.nlm.nih.gov/pubmed/22096332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-9668.71669 |
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