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Adrenomyeloneuropathy (AMN) is a rare genetic disease. In this study, a case of AMN was uncovered in a Chinese family. Click to show full abstract
Adrenomyeloneuropathy (AMN) is a rare genetic disease. In this study, a case of AMN was uncovered in a Chinese family.
Keywords:
chinese family;
family;
novel abcd1;
abcd1 gene;
gene mutation;
mutation causes
Journal Title: Brain and Behavior
Year Published: 2019
Link to full text (if available)
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Journal Title: Brain and Behavior
Year Published: 2019
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!