TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant

Nefrología - Tập 40 - Trang 91-98 - 2020
Miriam E. Reyna-Fabián1, Miguel A. Alcántara-Ortigoza1, Nancy L. Hernández-Martínez1, Jaime Berumen2,3, Raquel Jiménez-García4, Gilberto Gómez-Garza5, Ariadna González-del Angel1
1Laboratorio de Biología Molecular, Departamento de Genética Humana, Instituto Nacional de Pediatría, Secretaría de Salud, Ciudad de México, México
2Departamento de Medicina Experimental, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, México
3Unidad de Medicina Genómica, Hospital General de México, Ciudad de México, México
4Servicio de Nefrología, Instituto Nacional de Pediatría, Secretaría de Salud, Ciudad de México, México
5Resonancia Magnética, Instituto Nacional de Pediatría, Secretaría de Salud, Ciudad de México, México

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