Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation

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Bibliographic Details
Published in:International journal of hematology 2010-09, Vol.92 (2), p.405-408
Main Authors: Miyawaki, Yuhri, Suzuki, Atsuo, Fujimori, Yuhta, Takagi, Akira, Murate, Takashi, Suzuki, Nobuaki, Katsumi, Akira, Naoe, Tomoki, Yamamoto, Koji, Matsushita, Tadashi, Takamatsu, Junki, Kojima, Tetsuhito
Format: Article
Language:English
Subjects:
Biological and medical sciences
Chromosome Inversion
Factor VIII - genetics
Female
Hematologic and hematopoietic diseases
Hematology
Hemophilia A - genetics
Humans
Introns
Letter to the Editor
Medical sciences
Medicine
Medicine & Public Health
Oncology
Phenotype
Platelet diseases and coagulopathies
X Chromosome Inactivation
Young Adult
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ISSN:0925-5710
1865-3774
DOI:10.1007/s12185-010-0659-9