Statistics for Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports
Total visits
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| Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports | 154 |
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| January 2024 | 0 |
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| 13256_2018_Article_1702.pdf | 17 |
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