REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

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第一作者： Ingrid,Tein

第一单位： Division of Neurology, Department of Pediatrics, Laboratory Medicine and Pathobiology, The Hospital for Sick Children, University of Toronto, Toronto, Ont., Canada M5G 1X8.

作者： Ingrid,Tein ^[1] ; Orly,Elpeleg ; Bruria,Ben-Zeev ; Stanley H,Korman ; Alexander,Lossos ; Dorit,Lev ; Tally,Lerman-Sagie ; Gerard,Vockley ; Gerard T,Berry ; Anne-Marie,Lamhownah ; Dieter,Matern ; Charles R,Roe ; Niels,Gregersen

作者单位： Division of Neurology, Department of Pediatrics, Laboratory Medicine and Pathobiology, The Hospital for Sick Children, University of Toronto, Toronto, Ont., Canada M5G 1X8. ^[1]

DOI 10.1016/j.ymgme.2006.11.011

PMID 17234443

发布时间 2024-02-27

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Molecular genetics and metabolism

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REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

Molecular genetics and metabolism

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Molecular genetics and metabolism

相关期刊

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REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C&gt;T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

Molecular genetics and metabolism

相似文献

Molecular genetics and metabolism

相关期刊

检索历史清除

REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.