K. Rjiba, N. Soyah, M. Kammoun, I. Hadj Hmida, A. Saad, K. Mcelreavey, S. Mougou-Zerelli
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Élargissement du spectre phénotypique du syndrome meds (microcéphalie, épilepsie et diabète néonatal) lié au gène IER3IP1 : à propos d’un cas Tunisien présentant un hypogonadisme