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1. Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin.

Author

Cassereau J, Lavigne C, Letournel F, Ghali A, Verny C, Dubas F, Devière F, and Nicolas G

Subjects
Africa, Aged, Amyloid Neuropathies, Familial pathology, Asthenia genetics, Ataxia genetics, Cardiomyopathies genetics, Carpal Tunnel Syndrome genetics, Cognition Disorders genetics, Humans, Male, Mutation, Polyneuropathies genetics, Amyloid Neuropathies, Familial genetics, Amyloid Neuropathies, Familial physiopathology, Prealbumin genetics
Published
2008
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