Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene

Yoshinori Nishimoto; Hiroko Morisaki; Osamu Yamada; Yuichi Ichinose; Norihiro Suzuki

doi:10.1111/ncn3.102

Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene

Yoshinori Nishimoto, Hiroko Morisaki, Osamu Yamada, Yuichi Ichinose, Norihiro Suzuki

Department of Internal Medicine

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English
Pages (from-to)	126-128
Number of pages	3
Journal	Neurology and Clinical Neuroscience
Volume	2
Issue number	4
DOIs	https://doi.org/10.1111/ncn3.102
Publication status	Published - 2014 Jan 1

ASJC Scopus subject areas

Clinical Neurology
Neurology

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10.1111/ncn3.102

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author = "Yoshinori Nishimoto and Hiroko Morisaki and Osamu Yamada and Yuichi Ichinose and Norihiro Suzuki",

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AU - Yamada, Osamu

AU - Ichinose, Yuichi

AU - Suzuki, Norihiro

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JO - Neurology and Clinical Neuroscience

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Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene

ASJC Scopus subject areas

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