Slowly progressing amyotrophic lateral sclerosis caused by H46R SOD1 mutation [4]

European Neurology

Volumn 58, Issue 1, 2007, Pages 57-58

  Holmøy, Trygve ^a   Bjørgo, Kathrine ^a   Roos, Per M ^a  

^a ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; HISTIDINE;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; CLINICAL FEATURE; DISEASE COURSE; GASTROCNEMIUS MUSCLE; GENE; GENE MUTATION; H46R SOD1 GENE; HUMAN; LETTER; LOW BACK PAIN; MOTOR NERVE CONDUCTION; MUSCLE ATROPHY; NEUROLOGIC EXAMINATION; PARESIS; POINT MUTATION; PRIORITY JOURNAL; PROGNOSIS;

EID: 34447132164     PISSN: 00143022     EISSN: None     Source Type: Journal    
DOI: 10.1159/000102170     Document Type: Letter

References (3)

1. Aoki M, Ogasawara M, Matsubara Y, Narisawa K, Nakumara S, Itoyama Y, Abe K: Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible subtype of familial ALS. J Neurol Sci 1994;126:77-83.
2. Andersen PM: Amyotrophic lateral sclerosis associated with muations in the CuZn superoxide dismutase gene. Curr Neurol Neurosci Rep 2006;6:37-46.
3. Arisato T, Okubo R, Arata H, Abe K, Fukada K, Sakoda S, Shimizu A, Qin XH, Izumo S, Osame M, Nakagawa M: Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutations in large Japanese families. Acta Neuropathol (Berl) 2003; 106: 561-568.