Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies-Reference-Cited by-同舟云学术

Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies

Published:2003-10-15 Issue:6 Volume:28 Page:715-721
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Conceição Isabel,Sales-Luis Maria Lurdes,De Carvalho Mamede,Evangelista Teresinha,Fernandes Rui,Paunio Tiina,Kangas Hannele,Coutinho Paula,Neves Carlos,Saraiva Maria João

Funder

Fundação para a Ciência e Tecnologia from Portugal

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference28 articles.

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3. Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy;Darras;Neurology,1986

4. Gelsolin-derived familial amyloidosis caused by asparaginase or tyrosine substitution for aspartic acid at residue 187;de la Chapelle;Nat Genet,1992

5. Gelsolin variant (Asn-187) in familial amyloidosis. Finnish type;Ghiso;Biochem J,1990

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