Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- 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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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment ; volume:19 ; number:1 ; day:20 ; month:7 ; year:2018 ; pages:1-6 ; date:12.2018
BMC medical genetics ; 19, Heft 1 (20.7.2018), 1-6, 12.2018
- Beteiligte Personen und Organisationen
-
Schrauwen, Isabelle
Chakchouk, Imen
Acharya, Anushree
Liaqat, Khurram
Irfanullah
Nickerson, Deborah A.
Bamshad, Michael J.
Shah, Khadim
Ahmad, Wasim
Leal, Suzanne M.
SpringerLink (Online service)
- DOI
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10.1186/s12881-018-0618-5
- URN
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urn:nbn:de:101:1-2018092322113185730312
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:35 MESZ
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Beteiligte
- Schrauwen, Isabelle
- Chakchouk, Imen
- Acharya, Anushree
- Liaqat, Khurram
- Irfanullah
- Nickerson, Deborah A.
- Bamshad, Michael J.
- Shah, Khadim
- Ahmad, Wasim
- Leal, Suzanne M.
- SpringerLink (Online service)
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