Ceccarini, G., Magno, S., Pelosini, C., Ferrari, F., Sessa, M. R., Scabia, G., . . . Santini, F. (2020). Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease. Front Endocrinol (Lausanne).
Citação norma ChicagoCeccarini, Giovanni, et al. "Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease." Front Endocrinol (Lausanne) 2020.
Citação norma MLACeccarini, Giovanni, et al. "Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease." Front Endocrinol (Lausanne) 2020.