Anticipation in familial amyotrophic lateral sclerosis with SOD1-G93S mutation [1]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 72, Issue 6, 2002, Pages 819-820

  Iwai, K ^a   Yamamoto, M ^a   Yoshihara, T ^a   Sobue, G ^a  

^a NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE DURATION; FAMILIAL DISEASE; GENE MUTATION; HEREDITY; HUMAN; LETTER; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM;

ADULT; AGE OF ONSET; AGED; AMYOTROPHIC LATERAL SCLEROSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; SUPEROXIDE DISMUTASE;

EID: 0036265357     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.72.6.819     Document Type: Letter

References (6)

1. Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: Correlation between genotype and clinical features
2. Clustering of ALS patients in central Italy due to the occurrence of the L84F SOD1 gene mutation
3. Prognosis in familial amyotrophic lateral sclerosis: Progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutase
4. Anticipation in early- but not late-onset familial amyloid polyneuropathy (TTR Met30) in Japan
5. Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease
6. Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene