Articles with "cnot1 variant" as a keyword



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A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly.

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Published in 2019 at "American journal of human genetics"

DOI: 10.1016/j.ajhg.2019.03.017

Abstract: Holoprosencephaly is the incomplete separation of the forebrain during embryogenesis. Both genetic and environmental etiologies have been determined for holoprosencephaly; however, a genetic etiology is not found in most cases. In this report, we present… read more here.

Keywords: subunit cnot1; transcription complex; cnot1; ccr4 transcription ... See more keywords