Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations

BACKGROUND: Primary hyperoxaluria type 1 (PH1) is an autosomal recessive inherited disorder of glyoxylate metabolism in which excessive oxalates are formed by the liver and excreted by the kidneys. Calcium oxalate crystallizes in the urine, leading to urolithiasis, nephrocalcinosis, and consequent r...

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Detalles Bibliográficos
Autores principales: Kanoun, Houda, Jarraya, Faiçal, Maalej, Bayen, Lahiani, Amina, Mahfoudh, Hichem, Makni, Fatma, Hachicha, Jamil, Fakhfakh, Faiza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625645/
https://www.ncbi.nlm.nih.gov/pubmed/28969594
http://dx.doi.org/10.1186/s12882-017-0719-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625645/
https://www.ncbi.nlm.nih.gov/pubmed/28969594
http://dx.doi.org/10.1186/s12882-017-0719-y

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