A novel homoplasmic mitochondrial DNA mutation (m.13376T>C, p.I347T) of MELAS presenting characteristic medial temporal lobe atrophy

Ryo Sasaki, Yasuyuki Ohta, Noriko Hatanaka, Koh Tadokoro, Emi Nomura, Jingwei Shang, Mami Takemoto, Nozomi Hishikawa, Toru Yamashita, Yoshio Omote, Eisaku Morimoto, Sanae Teshigawara, Jun Wada, Yu ichi Goto, Koji Abe

Research output: Contribution to journalLetter

1 Citation (Scopus)
Original languageEnglish
Article number116460
JournalJournal of the neurological sciences
Volume408
DOIs
Publication statusPublished - Jan 15 2020

Keywords

  • MELAS
  • brain atrophy
  • medial temporal lobe
  • mtDNA
  • mutation

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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