Annales d'Endocrinologie
 2015
DOI: 10.1016/j.ando.2015.07.078
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Les mutations du gène MKRN3 sont fréquemment retrouvées dans les pubertés précoces centrales idiopathiques (PPC i) familiales

Dominique Simon
1
,
Ibrahima Ba
2
,
Nancy Mekhail
3
et al.
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