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Article

GREB1L as a candidate gene of Mayer-Rokitansky-Küster-Hauser Syndrome.

European journal of medical genetics - 1 Mar 2021

Kyei Barffour Isaac, Kyei Baah Kwarkoh Roselind

Abstract excerpt

Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome is a sex development disorder that affects 1 in every 4500 46, XX live births. At least a subset of MRKH syndrome is genetically related to which various candidate genes have been identified. The growth regulation by estrogen in breast cancer 1-like gene (GREB1L) is an androgen-regulated gene reported to be a co-activator of the retinoic acid receptor gene (RAR)....

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PMID: 33548512
DOI: 10.1016/j.ejmg.2021.104158

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GREB1L as a candidate gene of Mayer-Rokitansky-Küster-Hauser Syndrome.PMID 33548512Read ↗

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A Gene Implicated in Activation of Retinoic Acid Receptor Targets Is a Novel Renal Agenesis Gene in HumansSemantic proximity Read ↗

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Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implicationsSemantic proximity Read ↗

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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSemantic proximity Read ↗

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