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A case report of NPHP1 deletion in Chinese twins with nephronophthisis.
Chen, Feng; Dai, Limeng; Zhang, Jun; Li, Furong; Cheng, Jinbo; Zhao, Jinghong; Zhang, Bo.
Afiliação
  • Chen F; Department of Nephrology, the key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Kidney Center of PLA, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, 400037, China.
  • Dai L; Department of Medical Genetics, Army Medical University (Third Military Medical University), Chongqing, 400038, China.
  • Zhang J; Department of Nephrology, the key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Kidney Center of PLA, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, 400037, China.
  • Li F; Department of Nephrology, the key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Kidney Center of PLA, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, 400037, China.
  • Cheng J; Department of Nephrology, the key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Kidney Center of PLA, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, 400037, China.
  • Zhao J; Department of Nephrology, the key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Kidney Center of PLA, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, 400037, China.
  • Zhang B; Department of Nephrology, the key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Kidney Center of PLA, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, 400037, China. bo_zhang@tmmu.edu.cn.
BMC Med Genet ; 21(1): 84, 2020 04 19.
Article em En | MEDLINE | ID: mdl-32306954
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Proteínas do Citoesqueleto / Proteínas Adaptadoras de Transdução de Sinal / Doenças Renais Císticas / Falência Renal Crônica Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Proteínas do Citoesqueleto / Proteínas Adaptadoras de Transdução de Sinal / Doenças Renais Císticas / Falência Renal Crônica Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article