Novel compound heterozygous mutations in CNGA1in a Chinese family affected with autosomal recessive retinitis pigmentosa by targeted sequencing
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2415
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
-
Novel compound heterozygous mutations in CNGA1in a Chinese family affected with autosomal recessive retinitis pigmentosa by targeted sequencing ; volume:16 ; number:1 ; day:8 ; month:7 ; year:2016 ; pages:1-7 ; date:12.2016
BMC ophthalmology ; 16, Heft 1 (8.7.2016), 1-7, 12.2016
- Urheber
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Wang, Min
- Beteiligte Personen und Organisationen
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Gan, Dekang
Huang, Xin
Xu, Gezhi
SpringerLink (Online service)
- DOI
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10.1186/s12886-016-0281-6
- URN
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urn:nbn:de:1111-2016071124802
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:00 MESZ
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Beteiligte
- Wang, Min
- Gan, Dekang
- Huang, Xin
- Xu, Gezhi
- SpringerLink (Online service)
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