טוען...
A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD
The research on laminin α2 chain-deficient congenital muscular dystrophy (LAMA2-CMD) advanced rapidly in the last few decades, largely due to availability of good mouse models for the disease and a strong interest in preclinical studies from scientists all over the world. These mouse models continue...
שמור ב:
| הוצא לאור ב: | Front Mol Neurosci |
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| Main Authors: | , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Frontiers Media S.A.
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7188397/ https://ncbi.nlm.nih.gov/pubmed/32457577 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2020.00059 |
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