A novel deep intronic variant strongly associates with Alkaptonuria

Alkaptonuria is a rare autosomal recessive inherited disorder of tyrosine metabolism, which causes ochronosis, arthropathy, cardiac valvular calcification, and urolithiasis. The epidemiology of alkaptonuria in East Asia is not clear. In this study, patients diagnosed with alkaptonuria from January 2...

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Detalles Bibliográficos
Autores principales: Lai, Chien-Yi, Tsai, I-Jung, Chiu, Pao-Chin, Ascher, David B., Chien, Yin-Hsiu, Huang, Yu-Hsuan, Lin, Yi-Lin, Hwu, Wuh-Liang, Lee, Ni-Chung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536767/
https://www.ncbi.nlm.nih.gov/pubmed/34686677
http://dx.doi.org/10.1038/s41525-021-00252-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536767/
https://www.ncbi.nlm.nih.gov/pubmed/34686677
http://dx.doi.org/10.1038/s41525-021-00252-2

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