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(The University of Adelaide), Harald Stenmark(Norwegian Cancer Society), Annabel Whibley, Gillian Turner(Hunter Genetics), Patrick Tarpey(Wellcome Sanger Institute), Roger E. Stevenson(Piedmont Technical College), Andrés Server(Oslo University Hospital), Hans Sjöholm(Oslo University Hospital), Raffaella Smith(Wellcome Sanger Institute), Michael R. Stratton(Wellcome Sanger Institute), P. Andrew Futreal(Wellcome Sanger Institute), 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(University of Cambridge), Mette Kroken(Oslo University Hospital), Morten Mattingsdal(Oslo University Hospital), Jon W. Teague(Wellcome Sanger 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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