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An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth
Charcot-Marie Tooth (CMT) is a clinically and genetically heterogeneous group of diseases with rough genotype–phenotype correlation, so the final diagnosis requires extensive clinical and electrophysiological examination, family data, and gene mutation analysis. Although there is a common pattern of...
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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Mary Ann Liebert, Inc.
2013
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3525895/ https://ncbi.nlm.nih.gov/pubmed/23163601 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2012.0238 |
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