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Glutaric aciduria; a "new" disorder of amino acid metabolism.

作者信息

Goodman S I, Markey S P, Moe P G, Miles B S, Teng C C

出版信息

Biochem Med. 1975 Jan;12(1):12-21. doi: 10.1016/0006-2944(75)90091-5.

DOI:10.1016/0006-2944(75)90091-5
PMID:1137568
Abstract
摘要

相似文献

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Glutaric aciduria; a "new" disorder of amino acid metabolism.戊二酸尿症;一种氨基酸代谢的“新”紊乱症。
Biochem Med. 1975 Jan;12(1):12-21. doi: 10.1016/0006-2944(75)90091-5.
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Glutaric aciduria: inherited deficiency of glutaryl-CoA dehydrogenase activity.戊二酸尿症:戊二酰辅酶A脱氢酶活性的遗传性缺乏。
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Ketotic episodes in glutaryl-CoA dehydrogenase deficiency (glutaric aciduria).
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Glutaric aciduria: clinical and laboratory findings in two brothers.戊二酸尿症:两兄弟的临床及实验室检查结果
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Glutaric aciduria in progressive choreo-athetosis.进行性舞蹈手足徐动症中的戊二酸尿症
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Vigabatrin in the treatment of glutaric aciduria type I.
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7
Significance of bound glutarate in the diagnosis of glutaric aciduria type I.
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8
Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds.
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Subdural hematomas and glutaric aciduria type I.硬膜下血肿与I型戊二酸尿症
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CT in glutaric aciduria.戊二酸血症的CT表现
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