Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)

Author:

Reilly M. M.,Adams D.,Davis M. B.,Said G.,Harding A. E.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Reference17 articles.

1. Almeida M de R, Sasaki H, Sasaki Y, Salvi F, Ferlini A, Costa PP, Saraiva MJ (1993) Haplotype analysis of different FAP individuals with methionine 30 mutation in Europe. Arq Med 3: 189?192

2. Andersson R (1970) Hereditary amyloidosis with polyneuropathy. Acta Med Scand 188:85?94

3. Andrade C (1952) A peculiar form of peripheral neuropathy: familial atypical generalised amyloidosis with special involvement of the peripheral nerves. Brain 75:408?427

4. Araki S, Kurihara T, Tawara S, Kuribayashi T (1980) Familial amyloidotic polyneuropathy in Japan. In: Glenner G, Costa PP, Freitas AF (eds) Amyloid and amyloidosis. Excerpta Medica, Amsterdam, pp 67?77

5. Benson MD II, Turpin JC, Lucotte G, Zeldenrust S, Benson MD (1993) A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family. J Med Genet 30:120?122

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