ATP11A causes autosomal-dominant progressive, non-syndromic auditory synaptopathy / auditory neuropathy
- Weitere Titel
-
ATP als Ursache einer autosomaldominanten, progressiven, nichtsyndromalen Auditorischen Synaptopathie / Auditorischen Neuropathie
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Hamburg, Universität Hamburg, Dissertation, 2021
- Schlagwort
-
Neuropathy
- Ereignis
-
Veröffentlichung
- (wo)
-
Hamburg
- (wer)
-
Staats- und Universitätsbibliothek Hamburg Carl von Ossietzky
- (wann)
-
2021
- Urheber
-
von Loh, Sarah Maria
- Beteiligte Personen und Organisationen
-
Kubisch, Christian
- URN
-
urn:nbn:de:gbv:18-ediss-95624
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 07:19 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
- von Loh, Sarah Maria
- Kubisch, Christian
- Staats- und Universitätsbibliothek Hamburg Carl von Ossietzky
Entstanden
- 2021
Ähnliche Objekte (12)
Auditory processing in individuals with auditory neuropathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Genetic Defects Underlie the Non-syndromic Autosomal Recessive Intellectual Disability (NS-ARID)
Cortical auditory evoked potentials in peripheral neuropathy
Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss
A comparative study of auditory and non-auditory characteristics of congenital, early, and late-onset auditory neuropathy spectrum disorder
Screening mutations of OTOFgene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy
Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
Multidisciplinary treatment of non-syndromic oligodontia
Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders
Auditory processing in individuals with auditory neuropathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Genetic Defects Underlie the Non-syndromic Autosomal Recessive Intellectual Disability (NS-ARID)
Cortical auditory evoked potentials in peripheral neuropathy
Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss
A comparative study of auditory and non-auditory characteristics of congenital, early, and late-onset auditory neuropathy spectrum disorder
Screening mutations of OTOFgene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy
Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
Multidisciplinary treatment of non-syndromic oligodontia
Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders
Auditory processing in individuals with auditory neuropathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Genetic Defects Underlie the Non-syndromic Autosomal Recessive Intellectual Disability (NS-ARID)
Cortical auditory evoked potentials in peripheral neuropathy
Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss
A comparative study of auditory and non-auditory characteristics of congenital, early, and late-onset auditory neuropathy spectrum disorder
Screening mutations of OTOFgene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy
Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
Multidisciplinary treatment of non-syndromic oligodontia