Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.

Hopp, Katharina; Cogal, Andrea G; Bergstralh, Eric J; Seide, Barbara M; Olson, Julie B; Meek, Alicia M; Lieske, John C; Milliner, Dawn S; Harris, Peter C

Hopp, Katharina; Cogal, Andrea G; Bergstralh, Eric J; Seide, Barbara M; Olson, Julie B; Meek, Alicia M; Lieske, John C; Milliner, Dawn S; Harris, Peter C.

Hopp K; Division of Nephrology and Hypertension.
Cogal AG; Division of Nephrology and Hypertension.
Bergstralh EJ; Division of Biomedical Statistics and Informatics.
Seide BM; Division of Nephrology and Hypertension.
Olson JB; Division of Nephrology and Hypertension.
Meek AM; Division of Nephrology and Hypertension.
Lieske JC; Division of Nephrology and Hypertension.
Milliner DS; Division of Nephrology and Hypertension, Division of Pediatric Nephrology, Mayo Clinic, Rochester, Minnesota.
Harris PC; Division of Nephrology and Hypertension, Department of Biochemistry and Molecular Biology, and harris.peter@mayo.edu.

J Am Soc Nephrol ; 26(10): 2559-70, 2015 Oct.

Article en En | MEDLINE | ID: mdl-25644115

Asunto(s)

Estudios de Asociación Genética; Heterocigoto; Hiperoxaluria Primaria/genética; Adolescente; Adulto; Anciano; Niño; Preescolar; Humanos; Lactante; Persona de Mediana Edad; Adulto Joven

Palabras clave

genetic renal disease; kidney stones; molecular genetics

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hiperoxaluria Primaria / Estudios de Asociación Genética / Heterocigoto Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Humans / Infant / Middle aged Idioma: En Año: 2015 Tipo del documento: Article

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