Associated Papers
Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport.
Belville C et al.
Human Molecular Genetics, 2009
A 27 base-pair deletion of the anti-müllerian type II receptor gene is the most common cause of the persistent müllerian duct syndrome.
Imbeaud S et al.
Human Molecular Genetics, 1996
Surgical management and molecular diagnosis of persistent Müllerian duct syndrome in Chinese patients.
Tian HJ et al.
Asian Journal of Andrology, 0
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