Your browser doesn't support javascript.
loading
Characterization of the renal phenotype in RMND1-related mitochondrial disease.
Shayota, Brian J; Le, Nhon T; Bekheirnia, Nasim; Rosenfeld, Jill A; Goldstein, Amy C; Moritz, Michael; Bartholomew, Dennis W; Pastore, Matthew T; Xia, Fan; Eng, Christine; Yang, Yaping; Lamb, Dolores J; Scaglia, Fernando; Braun, Michael C; Bekheirnia, Mir Reza.
Afiliación
  • Shayota BJ; Texas Children's Hospital, Houston, TX, USA.
  • Le NT; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Bekheirnia N; Baylor College of Medicine, Houston, TX, USA.
  • Rosenfeld JA; Texas Children's Hospital, Houston, TX, USA.
  • Goldstein AC; Baylor College of Medicine, Houston, TX, USA.
  • Moritz M; Renal Section, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Bartholomew DW; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Pastore MT; Department of Pediatrics and Division of Child Neurology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Xia F; Department of Pediatrics, Division of Nephrology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Eng C; Division of Molecular and Human Genetics, Nationwide Children's Hospital, Columbus, OH, USA.
  • Yang Y; Division of Molecular and Human Genetics, Nationwide Children's Hospital, Columbus, OH, USA.
  • Lamb DJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Scaglia F; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Braun MC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Bekheirnia MR; Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
Mol Genet Genomic Med ; 7(12): e973, 2019 12.
Article en En | MEDLINE | ID: mdl-31568715
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Ciclo Celular / Enfermedades Mitocondriales / Enfermedades Renales / Mutación Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Screening_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Ciclo Celular / Enfermedades Mitocondriales / Enfermedades Renales / Mutación Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Screening_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos