Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codon
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference12 articles.
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4. X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management;Engelen;Orphanet J. Rare Dis.,2012
5. Frequent occurrence of cerebral demyelination in adrenomyeloneuropathy;de Beer;Neurology,2014
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1. A novel ABCD1 G1202A mutation in a Chinese patient with pure adrenomyeloneuropathy and literature review;Genes & Diseases;2021-09
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