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A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease.
Jafari Khamirani, Hossein; Palicharla, Vivek Reddy; Dastgheib, Seyed Alireza; Dianatpour, Mehdi; Imanieh, Mohammad Hadi; Tabei, Seyed Sajjad; Besse, Whitney; Mukhopadhyay, Saikat; Liem, Karel F.
Afiliação
  • Jafari Khamirani H; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Palicharla VR; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
  • Dastgheib SA; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dianatpour M; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Imanieh MH; Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Tabei SS; Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Besse W; Shiraz Nephro-Urology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Mukhopadhyay S; Department of Internal Medicine, Section of Nephrology, Yale School of Medicine, New Haven, CT, United States.
  • Liem KF; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Front Genet ; 13: 1021037, 2022.
Article em En | MEDLINE | ID: mdl-36276950

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article