Carrier detection for adrenoleukodystrophy by high-performance liquid chromatography
Author:
Publisher
Elsevier BV
Subject
Developmental Neuroscience,Neurology
Reference22 articles.
1. Adrenoleukodystrophy: Abnormality of very long-chain fatty acids in erythrocyte membrane phospholipids;Antoku;Neurology (Cleveland),1984
2. Adrenoleukodystrophy: Fatty acid analysis of total glycerophospholipids in erythrocyte membranes;Antoku;Acta Neurol. Scand.,1985
3. Antoku, Y., T. Sakai, K. Tsukamoto, K. Imanishi, Y. Ohtsuka, H. Iwashita, and I. Goto. A simple diagnostic method of adrenoleukodystrophy: Total fatty acid analysis of erythrocyte membranes. Clin. Chim. Acta., in press.
4. Linkage of adrenoleukodystrophy to a polymorphic DNA probe;Aubourg;Ann. Neurol.,1987
5. Quantitative release of fatty acids from lipids by a simple hydrolysis procedure;Aveldãno;J. Lipid Res.,1983
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Adrenoleukodystrophy: A correlation between saturated very long-chain fatty acids in mononuclear cells and phenotype;Annals of Neurology;1991-07
2. Chorea-acanthocytosis: Abnormal composition of covalently bound fatty acids of erythrocyte membrane proteins;Annals of Neurology;1991-06
3. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991
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