טוען...
DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2
A subtelomeric region, 4q35.2, is implicated in facioscapulohumeral muscular dystrophy (FSHD), a dominant disease thought to involve local pathogenic changes in chromatin. FSHD patients have too few copies of a tandem 3.3-kb repeat (D4Z4) at 4q35.2. No phenotype is associated with having few copies...
שמור ב:
| Main Authors: | , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2794184/ https://ncbi.nlm.nih.gov/pubmed/19820107 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkp833 |
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