First Report of Lysozyme Amyloidosis with p.F21L/T88N Amino Acid Substitutions in a Russian Family

Lysozyme amyloidosis is caused by an amino acid substitution in the sequence of this protein. In our study, we described a clinical case of lysozyme amyloidosis in a Russian family. In our work, we described in detail the histological changes in tissues that appeared as a result of massive depositio...

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Detalles Bibliográficos
Autores principales: Suvorina, Mariya Yu., Stepanova, Elena A., Rameev, Vilen V., Kozlovskaya, Lidiya V., Glukhov, Anatoly S., Kuznitsyna, Anastasiya A., Surin, Alexey K., Galzitskaya, Oxana V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572506/
https://www.ncbi.nlm.nih.gov/pubmed/37833900
http://dx.doi.org/10.3390/ijms241914453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572506/
https://www.ncbi.nlm.nih.gov/pubmed/37833900
http://dx.doi.org/10.3390/ijms241914453

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