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Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility.
Aprea, I; Wilken, A; Krallmann, C; Nöthe-Menchen, T; Olbrich, H; Loges, N T; Dougherty, G W; Bracht, D; Brenker, C; Kliesch, S; Strünker, T; Tüttelmann, F; Raidt, J; Omran, H.
Afiliación
  • Aprea I; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Wilken A; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Krallmann C; Department of Clinical and Surgical Andrology, Centre of Reproductive Medicine and Andrology, University Hospital Münster, Münster, Germany.
  • Nöthe-Menchen T; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Olbrich H; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Loges NT; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Dougherty GW; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Bracht D; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Brenker C; Centre of Reproductive Medicine and Andrology, University Hospital Münster, University of Münster, Münster, Germany.
  • Kliesch S; Department of Clinical and Surgical Andrology, Centre of Reproductive Medicine and Andrology, University Hospital Münster, Münster, Germany.
  • Strünker T; Centre of Reproductive Medicine and Andrology, University Hospital Münster, University of Münster, Münster, Germany.
  • Tüttelmann F; Institute of Reproductive Genetics, University of Münster, Münster, Germany.
  • Raidt J; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
  • Omran H; Department of General Pediatrics, University Hospital Münster, Münster, Germany.
Front Genet ; 14: 1117821, 2023.
Article en En | MEDLINE | ID: mdl-36873931
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Genet Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Genet Año: 2023 Tipo del documento: Article