Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes/Leigh syndrome overlap patient with a novel m. 3482A>G mutation in MT‐ND1-Reference-Cited by-同舟云学术

Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes/Leigh syndrome overlap patient with a novel m. 3482A>G mutation in MT‐ND1

Published:2020-12-09 Issue:1 Volume:41 Page:84-90
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Hayashi Yuichi¹,Iwasaki Yasushi²^ORCID,Yoshikura Nobuaki¹,Yamada Megumi¹,Kimura Akio¹,Inuzuka Takashi¹³,Miyahara Hiroaki²^ORCID,Goto Yuichi⁴,Nishino Ichizo⁵^ORCID,Yoshida Mari²,Shimohata Takayoshi¹^ORCID

Affiliation:

1. Department of Neurology Gifu University Graduate School of Medicine Gifu Japan

2. Department of Neuropathology, Institute for Medical Science of Aging Aichi Medical University Nagakute Japan

3. Department of Neurology Gifu Municipal Hospital Gifu Japan

4. Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience National Center of Neurology and Psychiatry Kodaira Japan

5. Department of Neuromuscular Research, National Institute of Neuroscience National Center of Neurology and Psychiatry Kodaira Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/neup.12709

Reference27 articles.

1. Mitochondrial Respiratory-Chain Diseases

2. Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?