Literature DB >> 24441349

A new Indian family affected by gelsolin amyloidosis.

Boby Varkey Maramattom1, Yasha T Chickabasaviah.   

Abstract

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Mesh：

Year:  2013        PMID： 24441349     DOI： 10.4103/0028-3886.125372

Source DB:  PubMed          Journal:  Neurol India        ISSN： 0028-3886            Impact factor:   2.117


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  3 in total

1.  The First Argentinian Family with Familial Amyloidosis of the Finnish Type.

Authors:  Francisco Lucero Saá; Federico Andrés Cremona; Natalia Ximena Mínguez; María Laura Igarzabal; Pablo Chiaradía
Journal:  Case Rep Ophthalmol       Date:  2017-08-31

2.  A new heterozygous G duplicate in exon1 (c.100dupG) of gelsolin gene causes Finnish gelsolin amyloidosis in a Chinese family.

Authors:  Xuemin Feng; Hui Zhu; Teng Zhao; Yanbo Hou; Jingyao Liu
Journal:  Brain Behav       Date:  2018-11-12       Impact factor: 2.708

3.  The role of gelsolin domain 3 in familial amyloidosis (Finnish type).

Authors:  Habiba Zorgati; Mårten Larsson; Weitong Ren; Adelene Y L Sim; Jan Gettemans; Jonathan M Grimes; Wenfei Li; Robert C Robinson
Journal:  Proc Natl Acad Sci U S A       Date:  2019-06-26       Impact factor: 11.205
  3 in total

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