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Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome Cover

Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome

Open Access
|May 2018

References

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    MaJWangLYangYMMaoCHWanXHNovel SE18 RAC1 mutations in a Chinese patient presenting with parkinsonism and dystoniaNeurol Sci2018doi: 10.1007/s10072-018-3247-z
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    RoebenBSchüleRRufSBenderBAlhaddadBBenkertTet alSERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large familyJ Med Genet2018553947doi: 10.1136/jmedgenet-2017-10462228916646
DOI: https://doi.org/10.5334/tohm.427 | Journal eISSN: 2160-8288
Language: English
Submitted on: Apr 28, 2018
Accepted on: May 3, 2018
Published on: May 29, 2018
Published by: Columbia University Libraries/Information Services
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2018 Josef Finsterer, Fulvio A. Scorza, Ana C. Fiorini, Carla A. Scorza, Antonio Carlos Almeida, published by Columbia University Libraries/Information Services
This work is licensed under the Creative Commons License.