- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2731-4383
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Dystrophin genetic variants and autism ; volume:2 ; number:1 ; day:24 ; month:3 ; year:2022 ; pages:1-19 ; date:12.2022
Discover mental health ; 2, Heft 1 (24.3.2022), 1-19, 12.2022
- Creator
-
Passos-Bueno, Maria Rita
Costa, Claudia Ismania Samogy
Zatz, Mayana
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s44192-022-00008-z
- URN
-
urn:nbn:de:101:1-2022052620092947083471
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:34 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
- Passos-Bueno, Maria Rita
- Costa, Claudia Ismania Samogy
- Zatz, Mayana
- SpringerLink (Online service)
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Verteilung von Punktmutationen im Dystrophin-Gen
Phenotypic effects of genetic variants associated with autism
Dystrophin Splice Variants Are Distinctly Localized in the Hippocampus
Both rare and common genetic variants contribute to autism in the Faroe Islands
Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
Expression of Dystrophin Dp71 Splice Variants Is Temporally Regulated During Rodent Brain Development
Common genetic variants, acting additively, are a major source of risk for autism
Common Genetic Variants Link the Abnormalities in the Gut-Brain Axis in Prematurity and Autism
Genetic Advances in Autism
Analysis of the dystrophin interactome
Maternally inherited genetic variants of CADPS 2 are present in Autism Spectrum Disorders and Intellectual Disability patients
Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits
Verteilung von Punktmutationen im Dystrophin-Gen
Phenotypic effects of genetic variants associated with autism
Dystrophin Splice Variants Are Distinctly Localized in the Hippocampus
Both rare and common genetic variants contribute to autism in the Faroe Islands
Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
Expression of Dystrophin Dp71 Splice Variants Is Temporally Regulated During Rodent Brain Development
Common genetic variants, acting additively, are a major source of risk for autism
Common Genetic Variants Link the Abnormalities in the Gut-Brain Axis in Prematurity and Autism
Genetic Advances in Autism
Analysis of the dystrophin interactome
Maternally inherited genetic variants of CADPS 2 are present in Autism Spectrum Disorders and Intellectual Disability patients
Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits