Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects (Q24633634)

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Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects
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    Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects (English)
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    Mao Fu
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    Maria de Fátima Paiva Baracho
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    Maria Goretti Do Nascimento Santos
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    José Brandão-Neto
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    Sandra Villares
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    Francesco S Celi
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    Bernardo L Wajchenberg
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    June 2004
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    89
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    6
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    2916-22
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