Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy - Vigouroux, C; Magré, J; Vantyghem, M C; Bourut, C; Lascols, O; Shackleton, S; Lloyd, D J; Guerci, B; Padova, G; Valensi, P; Grimaldi, A; Piquemal, R; et al. (Diabetes (New York, N.Y.), 2000)
Keywords: Adipose Tissue - pathology; Adolescent; Adult; Atrophy; Biological and medical sciences; Body fat; Child; Codon; Congenital diseases; Consanguinity; Diabetes; Disease; Errors of metabolism; Exons; Female; Genotype & phenotype; Heterozygote; Humans; Insulin resistance; Kinases; Lamin Type A; Lamins; Lipids (lysosomal enzyme disorders, storage diseases); Lipodystrophy - genetics; Male; Medical sciences; Metabolic diseases; Middle Aged; Mutation; Nuclear Proteins - genetics; Pancreatitis; Patients; Pedigree; Sex Characteristics; Womens health; Human; Skin disease; Nucleotide sequence; Family study; Sex; Gene organization; Congenital disease; Genetic disease; Lipoatrophy; Genetics; Lipodystrophy; Adipose tissue disorders; Mutation