Kyllerman, Mårten

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome

Gilfillan, G. D., Selmer, K. K., Roxrud, I., Smith, R., Kyllerman, M., Eiklid, K., Kroken, M., Mattingsdal, M., Egeland, T., Stenmark, H., et al. (2008) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 232

Pain, Balance, Activity, and Participation in Children With Hypermobility Syndrome

Schubert-Hjalmarsson, E., Öhman, A., Kyllerman, M., & Beckung, E. (2012) · Pediatric Physical Therapy

Connective tissue disorders researchMusculoskeletal pain and rehabilitation

Cited by 49

Juvenile galactosialidosis with attacks of neuropathic pain and absence of sialyloligosacchariduria

Darin, N., Kyllerman, M., Hård, A.-L., Nordborg, C., & Månsson, J.-E. (2009) · European Journal of Paediatric Neurology

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 25