Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease

Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease

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Veröffentlicht in:Frontiers in genetics 2017, Vol.8, p.143-143
Hauptverfasser: Lopes, Fátima, Soares, Gabriela, Gonçalves-Rocha, Miguel, Pinto-Basto, Jorge, Maciel, Patrícia
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container_end_page 143
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container_title Frontiers in genetics
container_volume 8
creator Lopes, Fátima
Soares, Gabriela
Gonçalves-Rocha, Miguel
Pinto-Basto, Jorge
Maciel, Patrícia
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doi_str_mv 10.3389/fgene.2017.00143
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source DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; PubMed Central Open Access
title Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease
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