Myoclonus-Dystonia Syndrome and E-Sarcoglycan Deficiency

J Gordon Millichap

doi:10.15844/pedneurbriefs-16-10-8

Myoclonus-Dystonia Syndrome and E-Sarcoglycan Deficiency

Pediatric Neurology Briefs

Volume 16 (2002): Issue 10

By: J Gordon Millichap

Open Access

|Oct 2002

Abstract

Clinical and genetic findings in 9 European families with myoclonus-dystonia syndrome (MDS) are reported from Ludwig-Maximilians-Universitat, Munich, Germany.

References

Asmus F Zimprich A Tezenas Du Montcel S Kabus C Deuschl G Kupsch A Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype Ann Neurol 2002 Oct 52 4 489 492 10.1002/ana.10325 12325078
Open DOI Search in Google Scholar Back to article

Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-16-10-8 | Journal eISSN: 2166-6482

Journal RSS Feed

Language: English

Page range: 78 - 79

Published on: Oct 1, 2002

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Myoclonus-Dystonia Syndrome,

E-Sarcoglycan,

Agoraphobia

© 2002 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 16 (2002): Issue 10