Molecular defects in haemophilia B: detection by direct restriction enzyme analysis
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb08008.x/fullpdf
Reference36 articles.
1. The gene structure of human anti-haemophilic factor IX.
2. Defective propeptide processing of blood clotting factor IX caused by mutation of arginine to glutamine at position −4
3. DIRECT CARRIER TESTING IN 14 FAMILIES WITH HAEMOPHILIA B
4. A novel beta-thalassemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNA
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