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A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. Lack of association of CGL with polymorphism in the lamin A/C Gene.
Clin Endocrinol (Oxf). 2001 Mar;54(3):412-4. doi: 10.1046/j.1365-2265.2001.1216c.x.
Clin Endocrinol (Oxf). 2001.
PMID: 11298098
Free PMC article.
No abstract available.
Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects.
Fu M, Kazlauskaite R, Baracho Mde F, Santos MG, Brandão-Neto J, Villares S, Celi FS, Wajchenberg BL, Shuldiner AR.
Fu M, et al.
J Clin Endocrinol Metab. 2004 Jun;89(6):2916-22. doi: 10.1210/jc.2003-030485.
J Clin Endocrinol Metab. 2004.
PMID: 15181077
Free PMC article.
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