Generalized Dystonia Due to <scp>KMT2B</scp> Mutation in a Patient with a Previous Diagnosis of Russell Silver Syndrome-Reference-Cited by-同舟云学术

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Generalized Dystonia Due to KMT2B Mutation in a Patient with a Previous Diagnosis of Russell Silver Syndrome

Published:2023-08 Issue:S3 Volume:10 Page:
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Heiser Heather¹,Smith Kaitlin¹,Duis Jessica²,Forbes Emily¹

Affiliation:

1. Department of Neurology University of Colorado Aurora Colorado USA

2. Department of Pediatrics Children's Hospital Colorado Aurora Colorado USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference10 articles.

1. Diagnosis and management of Silver–Russell syndrome: first international consensus statement

2. The search for the gene for Silver-Russell syndrome

3. A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene Region

4. Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome

5. Myoclonus-Dystonia Due to Maternal Uniparental Disomy

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1. Preface to the 4th MDS Video Challenge Case Supplement for Movement Disorders Clinical Practice;Movement Disorders Clinical Practice;2023-08

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