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 journalComment/debate

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

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

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