Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2194-7791
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis ; volume:8 ; number:1 ; day:4 ; month:10 ; year:2021 ; pages:1-6 ; date:12.2021
Molecular and Cellular Pediatrics ; 8, Heft 1 (4.10.2021), 1-6, 12.2021
- Urheber
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s40348-021-00122-y
- URN
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urn:nbn:de:101:1-2021112918333776527026
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 07:32 MESZ
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Beteiligte
- Vidic, Clara
- Zaniew, Marcin
- Jurga, Szymon
- Thiele, Holger
- Reutter, Heiko
- Hilger, Alina Christine
- SpringerLink (Online service)
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