A mutation inactivating the distal SF1 binding site on the human anti-Müllerian hormone promoter causes persistent Müllerian duct syndrome Acknowledgments and Funding

Autor: Schteingart, Helena, Picard, Jean-Yves, Valeri, Clara, Marshall, Ian, Treton, Dominique, Di Clemente, Nathalie, Rey, Rodolfo, JOSSO, Nathalie

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz147/5522632⟩
Human Molecular Genetics, 2019, ⟨10.1093/hmg/ddz147/5522632⟩

International audience; The persistent Müllerian duct syndrome (PMDS) is a 46,XY disorder of sexual development characterized by the persistence of Müllerian duct derivatives, uterus and tubes, in otherwise normally masculinized males. The conditio

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Functional heterogeneity of nonresting B cells in human blood.

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Immunoregulatory functions of paf-acether. VI. Dual effect on human B cell proliferation.

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