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How to tackle the diagnosis of limb-girdle muscular dystrophy 2A
Limb-girdle muscular dystrophy (LGMD) 2A (calpainopathy) is the most frequent form of LGMD in many European countries. The increasing demand for a molecular diagnosis makes the identification of strategies to improve gene mutation detection crucial. We conducted both a quantitative analysis of calpa...
שמור ב:
| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Nature Publishing Group
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2986267/ https://ncbi.nlm.nih.gov/pubmed/18854869 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.193 |
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