Mette Kroken

SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome

Gregor D. Gilfillan, Kaja Kristine Selmer, Ingrid Roxrud et al. · The American Journal of Human Genetics · 2008 · 235 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +5

Friedreich ataxia in Norway – an epidemiological, molecular and clinical study

Iselin Marie Wedding, Mette Kroken, Sandra Pilar Henriksen et al. · Orphanet Journal of Rare Diseases · 2015 · 21 citations · Full text

Temple syndrome as a differential diagnosis to Prader–Willi syndrome: Identifying three new patients

Asgeir Lande, Mette Kroken, Kai Fr. Rabben et al. · American Journal of Medical Genetics Part A · 2017 · 17 citations

Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in <i><scp>ACVRL1</scp></i>

Ketil Heimdal, Bjørn Dalhus, Olaug K. Rødningen et al. · Clinical Genetics · 2015 · 14 citations

Norwegian Families, Genetic Testing, Mendelian Disorder +12