Correction: Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Correction: Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder ; volume:10 ; number:1 ; day:15 ; month:11 ; year:2023 ; pages:1 ; date:12.2023
Human genome variation ; 10, Heft 1 (15.11.2023), 1, 12.2023

Creator: Sonoyama, Toru
Ishino, Takashi
Ogawa, Yui
Oda, Takashi
Takeno, Sachio

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41439-023-00249-6

URN: urn:nbn:de:101:1-2024032510382627418792

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:49 AM CEST

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Sonoyama, Toru
Ishino, Takashi
Ogawa, Yui
Oda, Takashi
Takeno, Sachio
SpringerLink (Online service)

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Therapieansätze für Nonsense-Mutationen bei Succinat-Semialdehyd-Dehydrogenase-Defizit

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Correction: Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder

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Other Objects (12)

Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder

Therapieansätze für Nonsense-Mutationen bei Succinat-Semialdehyd-Dehydrogenase-Defizit

Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution

Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK

An immunocompetent patient with a nonsense mutation in NHEJ1 gene

Adenine phosphoribosyltransferase (APRT) deficiency: identification of a novel nonsense mutation

Combined immunodeficiency caused by a novel nonsense mutation in LCK

Autism spectrum disorder

Ataluren treatment of patients with nonsense mutation dystrophinopathy: ataluren for dystrophinopathy

"Pernicious nonsense"

Nonsense verse

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Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder

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Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution

Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK

An immunocompetent patient with a nonsense mutation in NHEJ1 gene

Adenine phosphoribosyltransferase (APRT) deficiency: identification of a novel nonsense mutation

Combined immunodeficiency caused by a novel nonsense mutation in LCK

Autism spectrum disorder

Ataluren treatment of patients with nonsense mutation dystrophinopathy: ataluren for dystrophinopathy

"Pernicious nonsense"

Nonsense verse

Nonsense novels

Identification of a novel nonsense NOG mutation in a patient with stapes ankylosis and symphalangism spectrum disorder

Therapieansätze für Nonsense-Mutationen bei Succinat-Semialdehyd-Dehydrogenase-Defizit

Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution

Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK

An immunocompetent patient with a nonsense mutation in NHEJ1 gene

Adenine phosphoribosyltransferase (APRT) deficiency: identification of a novel nonsense mutation

Combined immunodeficiency caused by a novel nonsense mutation in LCK

Autism spectrum disorder

Ataluren treatment of patients with nonsense mutation dystrophinopathy: ataluren for dystrophinopathy

"Pernicious nonsense"

Nonsense verse

Nonsense novels

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