Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Clin Genet
; 96(5): 402-410, 2019 11.
Article
en En
| MEDLINE
| ID: mdl-31328266
Palabras clave
chronic kidney disease (CKD); congenital anomalies of the kidney and urinary tract (CAKUT); genetics; nephronophthisis (NPHP); polycystic kidney disease PKD; renal disease; singleton-WES; steroid-resistant nephrotic syndrome (SRNS); targeted gene sequence (TGS); trio approach for WES (trio-WES); whole-exome sequence (WES)
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Predisposición Genética a la Enfermedad
/
Enfermedades Renales Quísticas
/
Insuficiencia Renal Crónica
/
Exoma
Tipo de estudio:
Clinical_trials
/
Diagnostic_studies
/
Etiology_studies
/
Incidence_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Límite:
Child
/
Child, preschool
/
Female
/
Humans
/
Male
País/Región como asunto:
Asia
Idioma:
En
Revista:
Clin Genet
Año:
2019
Tipo del documento:
Article
País de afiliación:
China