Chapter 1 Profiling of Mutations in the F8 and F9, Causative Genes of Hemophilia a and Hemophilia B"

doi 10.5772/26489
Full Text
Abstract

Available in full text

Date
Authors
Publisher

InTech

Related search

Hemophilia A: Different Phenotypes May Be Explained by Multiple and Variable Effects of the Causative Mutation in the F8 Gene

Haematologica
Hematology
2018English

Sixteen Novel Hemophilia a Causative Mutations in the First Argentinian Series of Severe Molecular Defects

Haematologica
Hematology
2007English

Severe Hemophilia B

2020English

Mutations at Arginine Residues in Two Asian Hemophilia B Patients

Nucleic Acids Research
Genetics
1990English

Delayed HIV-1 Seroconversion in a Hemophilia B Patient in Japan.

Journal of the Japan Society of Blood Transfusion
1991English

44 Aspects of Prenatal Diagnosis in Hemophilia a (Ha) and B (Hb)

Pediatric Research
Child HealthPediatricsPerinatology
1994English

Hemophilia B Acquired Through Liver Transplantation

Liver Transplantation
HepatologyTransplantationSurgery
2016English

Type 1 Diabetes Mellitus and Acquired Hemophilia

Endocrine Abstracts
2016English

Hemophilia

American Society for Clinical Laboratory Science
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy