A novel ABCD1 gene mutation causes adrenomyeloneuropathy in a Chinese family

A novel ABCD1 gene mutation causes adrenomyeloneuropathy in a Chinese family

Abstract Background Adrenomyeloneuropathy (AMN) is a rare genetic disease. In this study, a case of AMN was uncovered in a Chinese family. Methods Clinical manifestations were collected and observed through medical records, physical examination, laboratory tests, and magnetic resonance imaging (MRI)...

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Bibliographic Details
Main Authors: Chao Wang, Hongchao Liu, Bing Han, Hui Zhu, Jingyao Liu
Format: Article
Language:English
Published: Wiley 2019-10-01
Series:Brain and Behavior
Subjects:
ABCD1
adrenomyeloneuropathy
Chinese family
missense mutation
X‐linked
Online Access:https://doi.org/10.1002/brb3.1416

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