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Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia.
Kim, Man Jin; Kim, Sheehyun; Chae, Seung Won; Lee, Seungbok; Yoon, Jihoon G; Kim, Boram; Lee, Jee-Soo; Chae, Jong Hee; Seong, Moon-Woo; Moon, Jangsup.
Afiliación
  • Kim MJ; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Kim S; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Chae SW; Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Lee S; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Yoon JG; Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Kim B; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Lee JS; Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Chae JH; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Seong MW; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Moon J; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
J Hum Genet ; 68(6): 369-374, 2023 Jun.
Article en En | MEDLINE | ID: mdl-36747106
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ciliar Tipo de estudio: Prevalence_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ciliar Tipo de estudio: Prevalence_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article