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Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome

Williams-Beuren syndrome (WBS) is a neurological disorder resulting from a microdeletion, typically 1.5 megabases in size, at 7q11.23. Atypical patients implicate genes at the telomeric end of this multigene deletion as the main candidates for the pathology of WBS in particular the unequal cognitive...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Hinsley, Timothy A., Cunliffe, Pamela, Tipney, Hannah J., Brass, Andrew, Tassabehji, May
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Cold Spring Harbor Laboratory Press 2004
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2286546/
https://ncbi.nlm.nih.gov/pubmed/15388857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1110/ps.04747604
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