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Neurotransmitters and Sodium Channelopathies; Possible Link?
Investigators from the University of British Columbia, Great Ormond Street Hospital for Children, and the National Hospital reported their findings on neurotransmitter deficiencies in two patients with mutations in voltage-gated sodium genes (SCN2A and SCN8A) discovered by whole exome sequencing.
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| izdano v: | Pediatr Neurol Briefs |
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| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Pediatric Neurology Briefs Publishers
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5681457/ https://ncbi.nlm.nih.gov/pubmed/29184379 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15844/pedneurbriefs-31-3-1 |
| Oznake: |
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