ALys amyloidosis caused by compound heterozygosity in Exon 2 (Thr70Asn) and Exon 4 (Trp112Arg) of the lysozyme gene-Reference-Cited by-同舟云学术

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ALys amyloidosis caused by compound heterozygosity in Exon 2 (Thr70Asn) and Exon 4 (Trp112Arg) of the lysozyme gene

Published:2005 Issue:1 Volume:27 Page:119-120
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Röcken Christoph,Becker Konrad,Fändrich Marcus,Schroeckh Volker,Stix Barbara,Rath Thomas,Kähne Thilo,Dierkes Jutta,Roessner Albert,Albert Franz Werner

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 51 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. Systemic diseases affecting the GI tract: A review of clinical and histopathologic manifestations;Annals of Diagnostic Pathology;2024-12

2. Furosemide Derails Human Lysozyme Fibrillation by Interacting with Aggregation Hot Spots: A Biophysical Comprehension;The Journal of Physical Chemistry B;2024-04-29

3. First Report of Lysozyme Amyloidosis with p.F21L/T88N Amino Acid Substitutions in a Russian Family;International Journal of Molecular Sciences;2023-09-22

4. Evaluating the inhibitory potential of natural compound luteolin on human lysozyme fibrillation;International Journal of Biological Macromolecules;2023-04

5. Lysozyme amyloidosis—a report on a large German cohort and the characterisation of a novel amyloidogenic lysozyme gene variant;Amyloid;2022-05-09

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