Identification of single-nucleotide polymorphisms in the human LPIN1 gene

Journal of Human Genetics

Volumn 47, Issue 7, 2002, Pages 370-372

  Cao, Henian ^a   Hegele, Robert A ^a  

^a ROBARTS RESEARCH INSTITUTE   (Canada)

Author keywords

Adipose tissue; Complex traits; Diabetes; Genomic DNA; Lipodystrophy; Sequencing

Indexed keywords

PRIMER DNA; LPIN1 PROTEIN, HUMAN; LPIN1 PROTEIN, MOUSE; NUCLEAR PROTEIN;

ARTICLE; BERARDINELLI SEIP COMPLETE LIPODYSTROPHY; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; FAMILIAL PARTIAL LIPODYSTROPHY; GENE; GENE AMPLIFICATION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; LIPODYSTROPHY; LPIN1 GENE; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PHENOTYPE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; ANIMAL; GENETICS; GENOTYPE; MOUSE;

MURINAE;

ANIMALS; GENOTYPE; HUMANS; LIPODYSTROPHY; MICE; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 0036305548     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380200052     Document Type: Article

References (7)

1. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
2. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34
3. Molecular basis of partial lipodystrophy and prospects for therapy
4. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
5. Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1
6. Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin
7. Adipose tissue deficiency, glucose intolerance, and increased atherosclerosis result from mutation in the mouse fatty liver dystrophy (fld) gene