Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in ADGRL3 (LPHN3) and Two Pseudogenes-Reference-Cited by-同舟云学术

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Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in ADGRL3 (LPHN3) and Two Pseudogenes

Published:2022-09 Issue: Volume:Volume 15 Page:125-131
ISSN:1178-704X
Container-title:The Application of Clinical Genetics
language:en
Short-container-title:TACG

Author:

Maurer Martin H^ORCID,Kohler Anja^ORCID,Hudemann Melanie,Jüngling Jerome,Biskup Saskia,Menzel Martin

Publisher

Informa UK Limited

Subject

Genetics (clinical),Genetics

Reference42 articles.

1. Cross-species models of attention-deficit/hyperactivity disorder and autism spectrum disorder

2. Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

3. Genetic Causes and Modifiers of Autism Spectrum Disorder

4. Identification of candidate intergenic risk loci in autism spectrum disorder

5. Genetics of glutamate and its receptors in autism spectrum disorder

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Shared Genetic Determinants of Schizophrenia and Autism Spectrum Disorder Implicate Opposite Risk Patterns: A Genome-Wide Analysis of Common Variants;Schizophrenia Bulletin;2024-04-14

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