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

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

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

Maurer, Martin H; Kohler, Anja; Hudemann, Melanie; Jüngling, Jerome; Biskup, Saskia; Menzel, Martin.

Afiliação

Maurer MH; Mariaberg Hospital for Child and Adolescent Psychiatry, Gammertingen, Germany.
Kohler A; Mariaberg Hospital for Child and Adolescent Psychiatry, Gammertingen, Germany.
Hudemann M; Mariaberg Hospital for Child and Adolescent Psychiatry, Gammertingen, Germany.
Jüngling J; Zentrum für Humangenetik, Tübingen, Germany.
Biskup S; Zentrum für Humangenetik, Tübingen, Germany.
Menzel M; Center for Genomics and Transcriptomics, CeGaT GmbH, Tübingen, Germany.

Appl Clin Genet ; 15: 125-131, 2022.

Article em En | MEDLINE | ID: mdl-36082049

Palavras-chave

ADGRL3; ASD; LPHN3; adhesion G protein-coupled receptor L3; autism spectrum disorder; latrophilin-3

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article