Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder

Heterozygous mutations of the HNF1B gene are the commonest known monogenic cause of developmental kidney disease. Half of patients have a deletion (approximately 1.3 Mb) of chromosome 17q12, encompassing HNF1B plus 14 additional genes. This 17q12 deletion has been linked with an increased risk of ne...

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Detalhes bibliográficos
Publicado no:Kidney Int
Main Authors: Clissold, Rhian L., Shaw-Smith, Charles, Turnpenny, Peter, Bunce, Benjamin, Bockenhauer, Detlef, Kerecuk, Larissa, Waller, Simon, Bowman, Pamela, Ford, Tamsin, Ellard, Sian, Hattersley, Andrew T., Bingham, Coralie
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2016
Assuntos:
Clinical Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4915913/
https://ncbi.nlm.nih.gov/pubmed/27234567
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.kint.2016.03.027
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