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Journal Article
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Journal Article
BMC Medical Genetics, ISSN 1471-2350, 09/2010, Volume 11, Issue 1, pp. 130 - 130
Background: Familial amyloidosis with polyneuropathy (FAP) is an autosomal dominant disease caused by transthyretin (TTR) mutations, of which V30M (TTR c.148G... 
SWEDEN | TARGET | OXIDATIVE STRESS | GEOGRAPHICAL-DISTRIBUTION | FAMILIAL AMYLOIDOTIC POLYNEUROPATHY | SEQUENCE | MUTATION | GENETICS & HEREDITY | SYSTEMIC AMYLOIDOSIS | BINDING | VAL30MET | Prealbumin - genetics | Amyloid Neuropathies, Familial - genetics | Gene Frequency | Humans | Middle Aged | Gene Silencing | Penetrance | Mutation, Missense | Sweden - epidemiology | Amyloid Neuropathies, Familial - epidemiology | Young Adult | Phenotype | Age of Onset | Alleles | Aged, 80 and over | Adult | Heterozygote | Aged | MicroRNAs - genetics | Polymorphism, Single Nucleotide | Proteins | MicroRNA | Gene mutations | Health aspects | Analysis | Oxidative stress | Genes | Manuscripts | Studies | Genotype & phenotype | Hospitals | Epigenetics | Writing | Genetic engineering | Mutation | Genetic testing | Binding sites | Acquisitions & mergers | Index Medicus | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Single Nucleotide; Transthyretin; 3' Untranslated Regions/genetics | MEDICINE | Klinisk genetik | Dermatology and venerology,clinical genetics, internal medicine | Medical Genetics | Medicinsk genetik | Allele Frequency; Amyloidosis; Amyloid Neuropathies | Clinical genetics | Familial; Humans; MicroRNA; Polymorphism | MEDICIN | Medicinska och farmaceutiska grundvetenskaper | genetik | Genetics | Dermatologi och venerologi, klinisk genetik, invärtesmedicin
Journal Article
Clinical Genetics, ISSN 0009-9163, 02/2009, Volume 75, Issue 2, pp. 163 - 168
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 12/2007, Volume 91, Issue 12, pp. 1607 - 1609
Journal Article
Clinica Chimica Acta, ISSN 0009-8981, 2008, Volume 398, Issue 1, pp. 10 - 14
Journal Article
Journal Article
Journal Article