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

Research output: Contribution to journal › Comment/debate

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

Cite this

@article{15ecab0fe350416eb47b0396dac2cb88,

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

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

year = "2014",

month = jan,

day = "1",

doi = "10.1111/ncn3.102",

language = "English",

volume = "2",

pages = "126--128",

journal = "Neurology and Clinical Neuroscience",

issn = "2049-4173",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "4",

}

TY - JOUR

T1 - Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene

AU - Nishimoto, Yoshinori

AU - Morisaki, Hiroko

AU - Yamada, Osamu

AU - Ichinose, Yuichi

AU - Suzuki, Norihiro

PY - 2014/1/1

Y1 - 2014/1/1

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U2 - 10.1111/ncn3.102

DO - 10.1111/ncn3.102

M3 - Comment/debate

VL - 2

SP - 126

EP - 128

JO - Neurology and Clinical Neuroscience

JF - Neurology and Clinical Neuroscience

SN - 2049-4173

IS - 4

ER -