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LIMK1 and CLIP‐115: linking cytoskeletal defects to Williams syndrome

21 Jan 2004

Abstract excerpt

Williams Syndrome is a developmental disorder that is characterized by cardiovascular problems, particular facial features and several typical behavioral and neurological abnormalities. In Williams Syndrome patients, a heterozygous deletion is present of a region on chromosome 7q11.23 (the Williams Syndrome critical region), which spans approximately 20 genes. Two of these genes encode proteins that regulate...

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PMID: 14745832
DOI: 10.1002/bies.10402

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