Expression Analysis and Protein Localization of the Human HPC-1/Syntaxin 1A, a Gene Deleted in Williams Syndrome
- 15 December 1999
- Vol. 62 (3), 525-528
- https://doi.org/10.1006/geno.1999.5987
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Williams–Beuren Syndrome: Unraveling the Mysteries of a Microdeletion DisorderMolecular Genetics and Metabolism, 1999
- Cerebellum and cerebrum in adaptive control and cognition: a reviewBiological Cybernetics, 1997
- Hemizygous Deletion of the Syntaxin 1A Gene in Individuals with Williams SyndromeAmerican Journal of Human Genetics, 1997
- Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosisHuman Molecular Genetics, 1997
- Novel isoform of syntaxin 1 is expressed in mammalian cellsBiochemical Journal, 1997
- Williams Syndrome: An Overview of Medical, Cognitive, and Behavioral FeaturesChild and Adolescent Psychiatric Clinics of North America, 1996
- LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive CognitionCell, 1996
- The syntaxin family of vesicular transport receptorsCell, 1993
- Hemizygosity at the elastin locus in a developmental disorder, Williams syndromeNature Genetics, 1993
- Natural history of Williams syndrome: Physical characteristicsThe Journal of Pediatrics, 1988