Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes

Differentiating between inherited renal hypouricemia and transient hypouricemic status is challenging. Here, we aimed to describe the genetic background of hypouricemia patients using whole-exome sequencing (WES) and assess the feasibility for genetic diagnosis using two founder variants in primary...

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Detalles Bibliográficos
Autores principales: Cha, Do Hyeon, Gee, Heon Yung, Cachau, Raul, Choi, Jong Mun, Park, Daeui, Jee, Sun Ha, Ryu, Seungho, Kim, Kyeong Kyu, Won, Hong-Hee, Limou, Sophie, Myung, Woojae, Winkler, Cheryl A., Cho, Sung Kweon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779878/
https://www.ncbi.nlm.nih.gov/pubmed/31591475
http://dx.doi.org/10.1038/s41598-019-50798-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779878/
https://www.ncbi.nlm.nih.gov/pubmed/31591475
http://dx.doi.org/10.1038/s41598-019-50798-6

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