The natural history of elevated tetradecenoyl-L-carnitine detected by newborn screening in New Zealand: implications for very long chain acyl-CoA dehydrogenase deficiency screening and treatment

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作者： Ryder, Bryony ^[1] ; Knoll, Detlef ^[2] ; Love, Donald R. ^[3] ; Shepherd, Phillip ^[4] ; Love, Jennifer M. ^[5] ; Reed, Peter W. ^[6] ; de Hora, Mark ; Webster, Dianne ; Glamuzina, Emma ; Wilson, Callum

作者单位： Auckland Uniserv Ltd Grafton, Auckland, New Zealand ^[1] Starship Childrens Hosp, Auckland, New Zealand ^[2] Auckland City Hosp, Newborn Metab Screening Unit, Auckland, New Zealand ^[3] Starship Childrens Hosp, Natl Metab Serv, POB 92024, Auckland, New Zealand ^[4] Auckland City Hosp, LabPLUS, Diagnost Genet, Auckland, New Zealand ^[5] Starship Childrens Hlth, Childrens Res Ctr, Auckland, New Zealand ^[6]

发布时间 2017-04-06

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Journal of inherited metabolic disease

2016年39卷3期

409-414页

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The natural history of elevated tetradecenoyl-L-carnitine detected by newborn screening in New Zealand: implications for very long chain acyl-CoA dehydrogenase deficiency screening and treatment

Journal of inherited metabolic disease

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Journal of inherited metabolic disease

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The natural history of elevated tetradecenoyl-L-carnitine detected by newborn screening in New Zealand: implications for very long chain acyl-CoA dehydrogenase deficiency screening and treatment

Journal of inherited metabolic disease

相似文献

Journal of inherited metabolic disease

相关期刊

检索历史清除