Carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlation
- PMID: 23520115
- DOI: 10.1002/humu.22286
Carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlation
Comment in
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Response to chen et Al.: carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlation.Hum Mutat. 2013 Apr;34(4):656. doi: 10.1002/humu.22285. Hum Mutat. 2013. PMID: 23520116 No abstract available.
Comment on
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Genotype-phenotype correlation in primary carnitine deficiency.Hum Mutat. 2012 Jan;33(1):118-23. doi: 10.1002/humu.21607. Epub 2011 Oct 11. Hum Mutat. 2012. PMID: 21922592 Free PMC article.
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Response to chen et Al.: carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlation.Hum Mutat. 2013 Apr;34(4):656. doi: 10.1002/humu.22285. Hum Mutat. 2013. PMID: 23520116 No abstract available.
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