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Clinical and genetic features of four patients with Pearson syndrome: An observational study.
Son, Ji Soo; Seo, Go Hun; Kim, Yoon-Myung; Kim, Gu-Hwan; Jin, Hee Kyung; Bae, Jae-Sung; Im, Ho Joon; Yoo, Han-Wook; Lee, Beom Hee.
Afiliación
  • Son JS; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, South Korea.
  • Seo GH; Division of Medical Genetics, 3billion Inc., Seoul, South Korea.
  • Kim YM; Department of Pediatrics, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, South Korea.
  • Kim GH; Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, South Korea.
  • Jin HK; Department of Laboratory Animal Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu, South Korea.
  • Bae JS; Department of Physiology, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, South Korea.
  • Im HJ; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, South Korea.
  • Yoo HW; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, South Korea.
  • Lee BH; Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, South Korea.
Medicine (Baltimore) ; 101(5): e28793, 2022 Feb 04.
Article en En | MEDLINE | ID: mdl-35119049
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Enfermedades Musculares Tipo de estudio: Observational_studies / Prognostic_studies / Screening_studies Límite: Child, preschool / Humans Idioma: En Revista: Medicine (Baltimore) Año: 2022 Tipo del documento: Article País de afiliación: Corea del Sur
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Enfermedades Musculares Tipo de estudio: Observational_studies / Prognostic_studies / Screening_studies Límite: Child, preschool / Humans Idioma: En Revista: Medicine (Baltimore) Año: 2022 Tipo del documento: Article País de afiliación: Corea del Sur