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A case of adrenomyeloneuropathy caused by a novel point mutation in the ABCD1 gene and functional verification

Xiaoxue Shi1,2,3, Xuelin Qi1,2, Jinhua Zheng1,2,3

  • 1Department of Neurology, Henan Provincial People's Hospital, Zhengzhou, China.

Frontiers in Genetics
|October 14, 2024
PubMed

Keywords:
ABCD1 geneadrenomyeloneuropathy (AMN)functional verificationgenetic analysispoint mutation

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