SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome
Gregor D. Gilfillan(Oslo University Hospital), Petter Strømme(Oslo University Hospital), Lena Samuelsson(University of Gothenburg), Jozef Gécz(South Australian Health and Medical Research Institute), Harald Stenmark(Oslo University Hospital), Annabel Whibley, Gillian Turner(Hunter Genetics), Patrick Tarpey(Wellcome Sanger Institute), Roger E. Stevenson(Atrium Health Wake Forest Baptist), Andrés Server(Oslo University Hospital), Hans Sjöholm(Oslo University Hospital), Raffaella Smith(Wellcome Sanger Institute), Michael R. Stratton(Wellcome Sanger Institute), P. Andrew Futreal(The University of Texas MD Anderson Cancer Center), Dag E. Undlien(Oslo University Hospital), Kristin Eiklid(Oslo University Hospital), Ingrid Roxrud(Norwegian Cancer Society), Charles E. Schwartz(Greenwood Genetic Center), Kaja Kristine Selmer(Oslo University Hospital), F. Lucy Raymond(Newcastle University), Mette Kroken(Oslo University Hospital), Morten Mattingsdal(Oslo University Hospital), Jon W. Teague(European Bioinformatics Institute), Arnold L. Christianson(National Health Laboratory Service), Thore Egeland(Oslo University Hospital), Mårten Kyllerman(Drottning Silvias barn- och ungdomssjukhus), Sarah Edkins(Wellcome Sanger Institute)
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