Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lis...
Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome
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Switzerland: Frontiers Research Foundation
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Language
English
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Switzerland: Frontiers Research Foundation
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Contents
is the main causative gene for lissencephaly, while
is the main causative gene for Rett syndrome, both of which are neurodevelopmental diseases. Here we report nuclear functions for LIS1 and identify previously unrecognized physical and genetic interactions between the products of these two genes in the cell nucleus, that has implications on MeC...
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Full title
Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome
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TN_cdi_doaj_primary_oai_doaj_org_article_40398585dc954a68afe2ed88884eb0a1
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_40398585dc954a68afe2ed88884eb0a1
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ISSN
1662-5102
E-ISSN
1662-5102
DOI
10.3389/fncel.2019.00370
