{Reference Type}: Journal Article
{Title}: Identification of one novel mutation in the EVC2 gene in a Chinese family with Ellis-van Creveld syndrome.
{Author}: Zhang Z;Bao K;He JW;Fu WZ;Zhang CQ;Zhang ZL;
{Journal}: Gene
{Volume}: 511
{Issue}: 2
{Year}: Dec 2012 15
{Factor}: 3.913
{DOI}: 10.1016/j.gene.2012.09.071
{Abstract}: Ellis-van Creveld syndrome (EvC) is a rare autosomal recessive skeletal dysplasia characterized by short limbs, short ribs, postaxial polydactyly, and dysplastic nails and teeth. It is caused by biallelic mutations in the EVC or EVC2 gene. Here, we identified a novel nonsense mutation p.W828X (c.2484G>A) in exon 14 and a recurrent nonsense mutation p. R399X (c.1195C>T) in exon 10 of EVC2 gene in a Chinese boy with EvC. Identification of a novel genotype in EvC will provide clues to the phenotype-genotype relations and may assist not only in the clinical diagnosis of EvC but also in the interpretation of genetic information used for prenatal diagnosis and genetic counseling.