Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome

BACKGROUND: Alport syndrome (AS; OMIM#308,940) is a hereditary kidney disease that progresses over time and is distinguished by hearing loss and ocular irregularities. The syndrome has three subtypes, namely X-linked (XL; OMIM#301,050), autosomal recessive (AR; OMIM#203,780), and autosomal dominant...

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Detalles Bibliográficos
Autores principales: Liang, Lei, Wu, Haotian, Cai, Zeyu, Zhao, Jianrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436629/
https://www.ncbi.nlm.nih.gov/pubmed/37596645
http://dx.doi.org/10.1186/s12920-023-01623-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436629/
https://www.ncbi.nlm.nih.gov/pubmed/37596645
http://dx.doi.org/10.1186/s12920-023-01623-7

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