- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Mitochondrial mutations in maternally inherited hearing loss ; volume:18 ; number:1 ; day:20 ; month:3 ; year:2017 ; pages:1-6 ; date:12.2017
BMC medical genetics ; 18, Heft 1 (20.3.2017), 1-6, 12.2017
- Keyword
-
Gehörlosigkeit
Ohrenkrankheit
Audiologie
Ohrenheilkunde
- Creator
-
Mutai, Hideki
- Contributor
-
Watabe, Takahisa
Kosaki, Kenjiro
Ogawa, Kaoru
Matsunaga, Tatsuo
SpringerLink (Online service)
- DOI
-
10.1186/s12881-017-0389-4
- URN
-
urn:nbn:de:1111-201704098510
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:49 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
- Mutai, Hideki
- Watabe, Takahisa
- Kosaki, Kenjiro
- Ogawa, Kaoru
- Matsunaga, Tatsuo
- SpringerLink (Online service)
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Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India
Associations of mitochondrial DNA 3777–4679 region mutations with maternally inherited essential hypertensive subjects in China
Tinnitus in patients with hearing loss due to mitochondrial DNA pathogenic variants
High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Gout with hearing loss
Hearing Loss in Mucopolysaccharidosis
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss
Hearing loss
Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China
Mitochondrial DNA 7908–8816 region mutations in maternally inherited essential hypertensive subjects in China
Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India
Associations of mitochondrial DNA 3777–4679 region mutations with maternally inherited essential hypertensive subjects in China
Tinnitus in patients with hearing loss due to mitochondrial DNA pathogenic variants
High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Gout with hearing loss