Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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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
- Contributor
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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
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:35 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- 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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