Most cases of familial amyloidotic polyneuropathy (FAP) are associated with amino acid substitutions destabilizing the folded state of transthyretin monomers-Reference-Cited by-同舟云学术

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Most cases of familial amyloidotic polyneuropathy (FAP) are associated with amino acid substitutions destabilizing the folded state of transthyretin monomers

Published:1996-02 Issue: Volume:6 Page:S17
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Altland K.,Benson M.D.,Ferlini A.,Husby G.,Linke R.P.,Salvi F.,Saraiva M.J.M.,Skinner M.,Sletten K.,Stainmetz A.,Winter P.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. On Typing Amyloidosis Using Immunohistochemistry. Detailled Illustrations, Review and a Note on Mass Spectrometry;Progress in Histochemistry and Cytochemistry;2012-08

2. Genetic microheterogeneity of human transthyretin detected by IEF;ELECTROPHORESIS;2007-06

3. Transthyretin Val71Ala mutation in a Dutch family with familial amyloidotic polyneuropathy;Amyloid;2000-01

4. Unusual Self-Association Properties of Transthyretin Y114C Related to Familial Amyloidotic Polyneuropathy: Effects on Detection and Quantification;Biochemical and Biophysical Research Communications;1999-08

5. A simple screening test for variant transthyretins associated with familial transthyretin amyloidosis using isoelectric focusing;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1998-09

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