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

International journal of hematology - 1 Sept 2010

Miyawaki Yuhri, Suzuki Atsuo, Fujimori Yuhta, Takagi Akira, Murate Takashi, Suzuki Nobuaki, Katsumi Akira, Naoe Tomoki, Yamamoto Koji, Matsushita Tadashi, Takamatsu Junki, Kojima Tetsuhito

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Share to Chromosome Inversion
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 20700669
DOI: 10.1007/s12185-010-0659-9

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Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation.PMID 20700669Read ↗

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