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 languageEnglish
Pages (from-to)126-128
Number of pages3
JournalNeurology and Clinical Neuroscience
Volume2
Issue number4
DOIs
Publication statusPublished - 2014 Jan 1

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Mutation
Genes
Osler-rendu-weber syndrome 2

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

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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. / 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

Nishimoto, Y, Morisaki, H, Yamada, O, Ichinose, Y & Suzuki, N 2014, 'Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene', Neurology and Clinical Neuroscience, vol. 2, no. 4, pp. 126-128. https://doi.org/10.1111/ncn3.102
Nishimoto Y, Morisaki H, Yamada O, Ichinose Y, Suzuki N. Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene. Neurology and Clinical Neuroscience. 2014 Jan 1;2(4):126-128. https://doi.org/10.1111/ncn3.102
Nishimoto, Yoshinori ; Morisaki, Hiroko ; Yamada, Osamu ; Ichinose, Yuichi ; Suzuki, Norihiro. / Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p. Thr52Pro), in the ALK1/ACVRL1 gene. In: Neurology and Clinical Neuroscience. 2014 ; Vol. 2, No. 4. pp. 126-128.
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