Frequencies and geographic distributions of genetic mutations in transthyretin- and non-transthyretin-related familial amyloidosis.

Zhen, D B; Swiecicki, P L; Zeldenrust, S R; Dispenzieri, A; Mauermann, M L; Gertz, M A

Zhen, D B; Swiecicki, P L; Zeldenrust, S R; Dispenzieri, A; Mauermann, M L; Gertz, M A.

Affiliation

Zhen DB; Department of Internal Medicine.
Swiecicki PL; Department of Internal Medicine.
Zeldenrust SR; Division of Hematology.
Dispenzieri A; Division of Hematology.
Mauermann ML; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Gertz MA; Division of Hematology.

Clin Genet ; 88(4): 396-400, 2015 Oct.

Article in En | MEDLINE | ID: mdl-25211232

Subject(s)

Amyloid Neuropathies, Familial/genetics; Genetic Predisposition to Disease/epidemiology; Prealbumin/genetics; DNA Mutational Analysis; Female; Genetic Testing; Geography; Humans; Male; Mutation, Missense; Retrospective Studies; United States/epidemiology

Key words

amyloidosis; apolipoprotein; fibrinogen; gelsolin; hereditary; lysozyme; mutation; transthyretin

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prealbumin / Genetic Predisposition to Disease / Amyloid Neuropathies, Familial Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: Clin Genet Year: 2015 Type: Article

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