Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu Zn superoxide dismutase gene: A possible new subtype of familial ALS

Masashi Aoki, Masahito Ogasawara, Yoichi Matsubara, Kuniaki Narisawa, Shozo Nakamura, Yasuto Itoyama, Koji Abe

研究成果: Article査読

97 被引用数 (Scopus)

抄録

Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurological disorder that results in relentless damage to the motor neuron system. Although about 5-10% of cases are familial, the pathophysiologic process of ALS remains unknown. We identified a novel point mutation A to G in exon 2 of the Cu Zn SOD gene, resulting in an amino acid substitution of histidine46 by arginine (H46R), in two Japanese familial ALS (FALS) families. The segregations of the mutation were evident. The enzymatic activities of Cu Zn SOD of peripheral red blood cell lysate were reduced to about 80% in the affected members, compared with other non-affected family members. The patients in these families are clinically characterized by relative late onset, initial involvement in lower extremities, relative rare impairment of bulbar muscles and much slow progression of muscular weakness and atrophy, compared with other Japanese FALS cases who have no mutation in the Cu Zn SOD gene. These findings suggest that the H46R mutation in Cu Zn SOD gene is highly related to this unique subtype of FALS.

本文言語English
ページ(範囲)77-83
ページ数7
ジャーナルJournal of the neurological sciences
126
1
DOI
出版ステータスPublished - 1994 10

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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