Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

Hemophilia B is an X-linked disease caused by a functional deficiency in coagulation factor IX. A cDNA clone corresponding to factor IX has been used to detect homologous sequences in the human genome. All DNA fragments hybridizing to the probe, under medium- or high-stringency conditions, are X-lin...

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Bibliografiska uppgifter
Huvudupphovsmän: Camerino, G, Grzeschik, K H, Jaye, M, De La Salle, H, Tolstoshev, P, Lecocq, J P, Heilig, R, Mandel, J L
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1984
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC344705/
https://ncbi.nlm.nih.gov/pubmed/6320191
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