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Autosomal recessive segregation of a truncating mutation of anti-Mullerian type II receptor in a family affected by the persistent Mullerian duct syndrome contrasts with its dominant negative activity in vitro.
Messika-Zeitoun, L.; Gouedard, L.; Belville, C. et al.
2001 • In Journal of Clinical Endocrinology and Metabolism, 86 (9), p. 4390-7

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