Expanding the spectrum of Grik2 mutations: intellectual disability, behavioural disorder, epilepsy and dystonia
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| Veröffentlicht in: | Clinical genetics 2015-03, Vol.87 (3), p.293-295 |
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| container_end_page | 295 |
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| container_issue | 3 |
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| container_title | Clinical genetics |
| container_volume | 87 |
| creator | Córdoba, M. Rodriguez, S. González Morón, D. Medina, N. Kauffman, M.A. |
| description | |
| doi_str_mv | 10.1111/cge.12423 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0009-9163 |
| ispartof | Clinical genetics, 2015-03, Vol.87 (3), p.293-295 |
| issn | 0009-9163 1399-0004 |
| language | eng |
| recordid | cdi_proquest_journals_1654885143 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | Adult Consanguinity Dystonia - diagnosis Dystonia - genetics Epilepsy - diagnosis Epilepsy - genetics Female Genome-Wide Association Study GluK2 Kainate Receptor Humans Intellectual Disability - diagnosis Intellectual Disability - genetics Male Mental Disorders - diagnosis Mental Disorders - genetics Mutation Pedigree Phenotype Receptors, Kainic Acid - genetics |
| title | Expanding the spectrum of Grik2 mutations: intellectual disability, behavioural disorder, epilepsy and dystonia |
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