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

Access to Document

10.1111/ncn3.102

Cite this

Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene. / Nishimoto, Yoshinori; Morisaki, Hiroko; Yamada, Osamu; Ichinose, Yuichi; Suzuki, Norihiro.

In: Neurology and Clinical Neuroscience, Vol. 2, No. 4, 01.01.2014, p. 126-128.

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

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