The defective splicing caused by the ISCU intron mutation in patients with myopathy with lactic acidosis is repressed by PTBP1 but can be derepressed by IGF2BP1 (Q82719408)
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scientific article published on 29 December 2011
Language | Label | Description | Also known as |
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English | The defective splicing caused by the ISCU intron mutation in patients with myopathy with lactic acidosis is repressed by PTBP1 but can be derepressed by IGF2BP1 |
scientific article published on 29 December 2011 |
Statements
The defective splicing caused by the ISCU intron mutation in patients with myopathy with lactic acidosis is repressed by PTBP1 but can be derepressed by IGF2BP1 (English)
Angelica Nordin
Elin Larsson
Monica Holmberg
29 December 2011