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Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination
Progressive limb spasticity and cerebellar ataxia are frequently found together in clinical practice and form a heterogeneous group of degenerative disorders that are classified either as pure spastic ataxia or as complex spastic ataxia with additional neurological signs. Inheritance is either autos...
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| Vydáno v: | Am J Hum Genet |
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| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5473715/ https://ncbi.nlm.nih.gov/pubmed/28575651 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2017.05.009 |
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