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Update on the Phenotypic Spectrum of Lesch-Nyhan Disease and its Attenuated Variants

Congenital deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT) results in a spectrum of clinical phenotypes. All of these phenotypes are associated with marked overproduction of uric acid and related problems such as hyperuricemia, urate nephrolithiasis, tophi, and gout. T...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Torres, Rosa J., Puig, Juan G., Jinnah, Hyder A.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2012
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3408650/
https://ncbi.nlm.nih.gov/pubmed/22198833
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11926-011-0231-5
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