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Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II
Hereditary sensory and autonomic neuropathy type II (HSANII) is an early-onset autosomal recessive disorder characterized by loss of perception to pain, touch, and heat due to a loss of peripheral sensory nerves. Mutations in hereditary sensory neuropathy type II (HSN2), a single-exon ORF originally...
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| Main Authors: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2398735/ https://ncbi.nlm.nih.gov/pubmed/18521183 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI34088 |
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