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Rapid‐Onset Dystonia‐Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation
Shranjeno v:
izdano v: | Mov Disord Clin Pract |
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Main Authors: | , , , , , , |
Format: | Artigo |
Jezik: | Inglês |
Izdano: |
John Wiley and Sons Inc.
2014
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Teme: | |
Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6353356/ https://ncbi.nlm.nih.gov/pubmed/30713883 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12122 |
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