A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family ; volume:18 ; number:1 ; day:2 ; month:7 ; year:2024 ; pages:1-11 ; date:12.2024
Human genomics ; 18, Heft 1 (2.7.2024), 1-11, 12.2024
- Urheber
-
Zhang, Luping
Zheng, Danya
Xu, Lian
Wang, Han
Zhang, Shuqiang
Shi, Jianhua
Jin, Nana
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s40246-024-00628-2
- URN
-
urn:nbn:de:101:1-2409202133075.869885868605
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:34 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Zhang, Luping
- Zheng, Danya
- Xu, Lian
- Wang, Han
- Zhang, Shuqiang
- Shi, Jianhua
- Jin, Nana
- SpringerLink (Online service)
Ähnliche Objekte (12)
Spatial Dependency in Nonstationary GEV Modelling of Extreme Precipitation over Great Britain
Function of Heterogeneous Nuclear Ribonucleoprotein U and related MicroRNAs in Human Coronary Artery Endothelial Cells and Endothelial Microparticles
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family
Multiple positive solutions to singular fractional differential equations with integral boundary conditions involving p−q $p-q$-order derivatives
Postnatal maternal separation affects hippocampal longterm potentiation in adult stressed rats : molecular and hormonal mechanisms
Sulfoximines with α ‐Ketoester Functionalities at Nitrogen from Cyanoacetates and Air
Successful treatment of Enterococcus gallinarum infection in a neonate with vancomycin: a case report
ATP11A causes autosomal-dominant progressive, non-syndromic auditory synaptopathy / auditory neuropathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss
Spatial Dependency in Nonstationary GEV Modelling of Extreme Precipitation over Great Britain
Function of Heterogeneous Nuclear Ribonucleoprotein U and related MicroRNAs in Human Coronary Artery Endothelial Cells and Endothelial Microparticles
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family
Multiple positive solutions to singular fractional differential equations with integral boundary conditions involving p−q $p-q$-order derivatives
Postnatal maternal separation affects hippocampal longterm potentiation in adult stressed rats : molecular and hormonal mechanisms
Sulfoximines with α ‐Ketoester Functionalities at Nitrogen from Cyanoacetates and Air
Successful treatment of Enterococcus gallinarum infection in a neonate with vancomycin: a case report
ATP11A causes autosomal-dominant progressive, non-syndromic auditory synaptopathy / auditory neuropathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss
Spatial Dependency in Nonstationary GEV Modelling of Extreme Precipitation over Great Britain
Function of Heterogeneous Nuclear Ribonucleoprotein U and related MicroRNAs in Human Coronary Artery Endothelial Cells and Endothelial Microparticles
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family
Multiple positive solutions to singular fractional differential equations with integral boundary conditions involving p−q $p-q$-order derivatives
Postnatal maternal separation affects hippocampal longterm potentiation in adult stressed rats : molecular and hormonal mechanisms
Sulfoximines with α ‐Ketoester Functionalities at Nitrogen from Cyanoacetates and Air
Successful treatment of Enterococcus gallinarum infection in a neonate with vancomycin: a case report
ATP11A causes autosomal-dominant progressive, non-syndromic auditory synaptopathy / auditory neuropathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene