1 | CLIP2, WBS
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| The Contribution of CLIP2 Haploinsufficiency to the Clinical Manifestations of the Williams-Beuren Syndrome.
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| Vandeweyer G, Van der Aa N, Reyniers E, Kooy RF.
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| Am J Hum Genet 90(6):1071-8. Epub 2012 May 17.
2012
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2 | WBS, LIMK1, CLIP2
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| Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.
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| Marenco S, Siuta MA, Kippenhan JS, Grodofsky S, Chang WL, Kohn P, Mervis CB, Morris CA, Weinberger DR, Meyer-Lindenberg A, Pierpaoli C, Berman KF.
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| Proc Natl Acad Sci U S A 104(38):15117-22. Epub 2007 Sep 7. 2007
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3 | CLIP2, CLIP1
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| Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice.
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| Hoogenraad CC, Koekkoek B, Akhmanova A, Krugers H, Dortland B, Miedema M, van Alphen A, Kistler WM, Jaegle M, Koutsourakis M, Van Camp N, Verhoye M, van der Linden A, Kaverina I, Grosveld F, De Zeeuw CI, Galjart N.
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| Nat Genet 32(1):116-27. 2002
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4 | CLIP2
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| The murine CYLN2 gene : genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region.
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| Hoogenraad CC, et al.
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| Genomics 53 : 348-358. 1998
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5 | CLIP2
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| CLIP-115, a novel brain-specific cytoplasmic linker protein, mediates the localization of dentritic lamellar bodies.
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| De Zeeuw CI, et al.
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| Neuron 19 : 1187-1199. 1997
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6 | CLIP2, EIF4H, ELN, GTF2IRD1, LAT2, LIMK1, RFC2, WBS, WBS, WBSCR2
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| Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.
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| Osborne LR, et al.
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| Genomics 36 : 328-336. 1996
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