Childhood onset progressive myoclonic dystonia due to a de novo KCTD17 splicing mutation
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Published in | Parkinsonism & related disorders Vol. 61; pp. 7 - 9 |
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Main Authors | , , , , , , , |
Format | Report |
Language | English |
Published |
01.04.2019
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Online Access | Get full text |
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Bibliography: | ObjectType-Correspondence-1 ObjectType-Case Study-4 content type line 59 SourceType-Reports-1 ObjectType-Undefined-2 ObjectType-Report-3 ObjectType-Article-5 |
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ISSN: | 1873-5126 |
DOI: | 10.1016/j.parkreldis.2019.01.004 |