Anticipation in early- but not late-onset familial amyloid polyneuropathy (TTR Met 30) in Japan

Neurology

Volumn 55, Issue 3, 2000, Pages 451-452

  Misu, K ^a   Hattori, N ^a   Ando, Y ^b   Ikeda, S ^c   Sobue, Gen ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^c SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID NEUROPATHY; ARTICLE; AUTONOMIC DYSFUNCTION; FAMILIAL DISEASE; HUMAN; JAPAN; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL;

EID: 0033838537     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.3.451-a     Document Type: Article

References (7)

1. Hereditary generalized amyloidosis with polyneurophaty: Clinicopathological study of 65 Japanese patients
2. Late-onset familial amyloid polyneuropathy type I. (transthyretin Met 30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan: Clinicopathological and genetic features
3. Change in the age at onset in patients with familial amyloidotic polyneuropathy type I
4. A pedigree analysis with minimised ascertainment bias shows anticipation in Met 30-transthyretin related familial amyloid polyneuropathy
5. Comparative stability and clearance of [Met 30] transthyretin and [Met 119] transthyretin
6. Anticipation of age at onset in familial amyloidotic polyneuropathy (Portuguese type)
7. Familial amyloidotic polyneurophaty in Sweden: A pedigree analysis