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An intragenic deletion of the factor IX gene in a family with hemophilia B.

A family of seven patients severely afflicted with hemophilia B has been studied for their factor IX genes through the use of factor IX cDNA and genomic DNA probes. The patients had detectable (less than 10% of normal) factor IX antigen in urine and no detectable inhibitors in sera to factor IX prot...

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Bibliografske podrobnosti
Main Authors: Chen, S H, Yoshitake, S, Chance, P F, Bray, G L, Thompson, A R, Scott, C R, Kurachi, K
Format: Artigo
Jezik:Inglês
Izdano: 1985
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC424334/
https://ncbi.nlm.nih.gov/pubmed/3001143
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