Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B-Reference-Cited by-同舟云学术

Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B

Published:2015-12 Issue:8 Volume:26 Page:866-868
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Kim Hee-Jung,Lee Ki-O,Yoo Ki-Young,Kim Sun-Hee,Kim Hee-Jin

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference17 articles.

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2. Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.;Kwon;Haemophilia,2008

3. Mutation analysis impact on the genetic counseling of sporadic hemophilia B families.;Bicocchi;Am J Med Genet A,2003

4. Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene.;Koeberl;Am J Hum Genet,1990

5. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations.;Attali;Thromb Haemost,1999

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3. The Clinical Genetics of Hemophilia B (Factor IX Deficiency);The Application of Clinical Genetics;2021-11

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