Deep intronic mutations are rarely a cause of hemophilia B
- 2 September 1999
- journal article
- letter
- Published by Hindawi Limited in Human Mutation
- Vol. 14 (3), 267-268
- https://doi.org/10.1002/(sici)1098-1004(1999)14:3<267::aid-humu11>3.0.co;2-i
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Reported in vivo splice-site mutations in the factor IX gene: Severity of splicing defects and a hypothesis for predicting deleterious splice donor mutationsHuman Mutation, 1999
- In a Blinded Analysis, Restriction Endonuclease Fingerprinting Detects All the Mutations in a 1.9-kb SegmentBioTechniques, 1997
- Complete nucleotide sequences of the gene for human factor IX (antihemophilic factor B)Biochemistry, 1985