A Mouse Mutation That Dysregulates Neighboring <i>Galnt17</i> and <i>Auts2</i> Genes Is Associated with Phenotypes Related to the Human AUTS2 Syndrome.

Weisner, P Anne; Chen, Chih-Ying; Sun, Younguk; Yoo, Jennifer; Kao, Wei-Chun; Zhang, Huimin; Baltz, Emily T; Troy, Joseph M; Stubbs, Lisa

A Mouse Mutation That Dysregulates Neighboring Galnt17 and Auts2 Genes Is Associated with Phenotypes Related to the Human AUTS2 Syndrome.

Weisner, P Anne; Chen, Chih-Ying; Sun, Younguk; Yoo, Jennifer; Kao, Wei-Chun; Zhang, Huimin; Baltz, Emily T; Troy, Joseph M; Stubbs, Lisa.

Affiliation

Weisner PA; Carl R. Woese Institute for Genomic Biology.
Chen CY; Neuroscience Program.
Sun Y; Carl R. Woese Institute for Genomic Biology.
Yoo J; Department of Cell and Developmental Biology, and.
Kao WC; Carl R. Woese Institute for Genomic Biology.
Zhang H; Department of Cell and Developmental Biology, and.
Baltz ET; Carl R. Woese Institute for Genomic Biology.
Troy JM; Carl R. Woese Institute for Genomic Biology.
Stubbs L; Carl R. Woese Institute for Genomic Biology.

G3 (Bethesda) ; 9(11): 3891-3906, 2019 11 05.

Article de En | MEDLINE | ID: mdl-31554716

Sujet(s)
Mots clés

Autism; Gene regulation; Neurological development; Syndromic phenotypes; Translocation

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription / N-acetylgalactosaminyltransferase / Protéines du cytosquelette Type d'étude: Prognostic_studies / Risk_factors_studies Limites: Animals / Female / Humans / Male Langue: En Journal: G3 (Bethesda) Année: 2019 Type de document: Article

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