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A new ATTR Phe64Ile mutation with late-onset multiorgan involvement.
- Source :
-
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2007 Dec; Vol. 14 (4), pp. 289-92. - Publication Year :
- 2007
-
Abstract
- We describe a novel transthyretin mutation in which phenylalanine is replaced with isoleucine in exon 3 at codon 64: Phe64Ile. The mutation was found in an isolated patient and it was not possible to perform a family study. The phenotype included heart and peripheral nerve involvement associated with a possible gastrointestinal and renal involvement.
- Subjects :
- Aged
Amyloidosis, Familial pathology
Base Sequence
Cardiomyopathies genetics
Cardiomyopathies pathology
Codon genetics
DNA Mutational Analysis
Echocardiography
Exons genetics
Humans
Isoleucine genetics
Male
Molecular Sequence Data
Phenylalanine genetics
Amyloidosis, Familial genetics
Mutation, Missense
Prealbumin genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1350-6129
- Volume :
- 14
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
- Publication Type :
- Academic Journal
- Accession number :
- 17968689
- Full Text :
- https://doi.org/10.1080/13506120701614172