Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families
- 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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Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families ; volume:14 ; number:1 ; day:17 ; month:7 ; year:2013 ; pages:1-7 ; date:12.2013
BMC medical genetics ; 14, Heft 1 (17.7.2013), 1-7, 12.2013
- Urheber
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Woo, Hae-Mi
- Beteiligte Personen und Organisationen
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Park, Hong-Joon
Baek, Jeong-In
Park, Mi-Hyun
Kim, Un-Kyung
Sagong, Borum
Koo, Soo Kyung
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-14-72
- URN
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urn:nbn:de:1111-2016071517167
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:55 MESZ
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Beteiligte
- Woo, Hae-Mi
- Park, Hong-Joon
- Baek, Jeong-In
- Park, Mi-Hyun
- Kim, Un-Kyung
- Sagong, Borum
- Koo, Soo Kyung
- SpringerLink (Online service)
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