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

Authors :: Cassereau J
Lavigne C
Letournel F
Ghali A
Verny C
Dubas F
Devière F
Nicolas G
Source :: Journal of the peripheral nervous system : JPNS [J Peripher Nerv Syst] 2008 Sep; Vol. 13 (3), pp. 251-4.
Publication Year :: 2008

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

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