Japanese triplets with cerebrotendinous xanthomatosis are homozygous for a mutant gene coding for the sterol 27-hydroxylase (Arg441Trp)
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Cited by 17 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. Differing clinical features between Japanese siblings with cerebrotendinous xanthomatosis with a novel compound heterozygous CYP27A1 mutation: a case report;BMC Neurology;2022-05-25
2. Neurologic findings are the sole manifestations of a patient with cerebrotendinous xanthomatosis;Neurology and Clinical Neuroscience;2019-03-27
3. Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series;Neurological Sciences;2016-11-25
4. Three siblings with Cerebrotendinous Xanthomatosis: A novel mutation in the CYP27A1 gene;European Journal of Medical Genetics;2012-01
5. Cerebrotendinous Xanthomatosis;Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes;2008
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