HPRT deficiency in a two-month-old child presentig acute renal failure and gout with a new deletion of two bases in exon 3 of the HPRT gene
Document title: HPRT deficiency in a two-month-old child presentig acute renal failure and gout with a new deletion of two bases in exon 3 of the HPRT gene
Journal: Archives of medical research
Database: PERIÓDICA
System number: 000264620
ISSN: 0188-4409
Authors: 1
2


3
Institutions: 1Hospital Infantil de México "Federico Gómez", Departamento de Pediatría, México, Distrito Federal. México
2Benemérita Universidad Autónoma de Puebla, Facultad de Medicina, Puebla. México
3University of Vermont, Genetics Laboratory, Burlington, Vermont. Estados Unidos de América
Year:
Season: May
Volumen: 38
Number: 4
Pages: 460-462
Country: México
Language: Inglés
Document type: Artículo
Approach: Caso clínico
Disciplines: Medicina
Keyword: Metabolismo y nutrición,
Nefrología,
Genética,
Hiperuricemia,
Insuficiencia renal aguda (IRA),
HPRT,
Gota,
Síndrome de Lesch-Nyhan
Keyword: Medicine,
Metabolism and nutrition,
Nephrology,
Hyperuricemia,
Acute renal failure (ARF),
HPRT,
Gout,
Lesch-Nyhan syndrome,
Genetics
Document request
Note: The document is shipping cost.









Original documents can be consulted at the Departamento de Información y Servicios Documentales, located in the Annex to the General Directorate of Libraries (DGB), circuito de la Investigación Científica across from the Auditorium Nabor Carrillo, located between the Institutes of Physics and Astronomy. Ciudad Universitaria UNAM. Show map
For more information: Departamento de Información y Servicios Documentales, Tels. (5255) 5622-3960, 5622-3964. E-mail: sinfo@dgb.unam.mx . Monday to Friday from (8 to 16 hrs).