Mutations in<i>Gng3lg</i>and<i>AGPAT2</i>in Berardinelli-Seip Congenital Lipodystrophy and Brunzell Syndrome: Phenotype Variability Suggests Important Modifier Effects
Mao Fu(University of Maryland, Baltimore), Alan R. Shuldiner(Regeneron (United States)), Maria Goretti do Nascimento Santos(Universidade Federal do Rio Grande do Norte), José Brandão‐Neto(Universidade Federal do Rio Grande do Norte), S M Villares(Universidade de São Paulo), Francesco S. Celi(UConn Health), Maria de Fátima Paiva Baracho(Universidade Federal do Rio Grande do Norte), Rasa Kazlauskaite(Rush University Medical Center), B L Wajchenberg(Institut national de recherche en sciences et technologies du numérique)
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