A novel mutation in the ABCD1 gene of a Chinese patient with X-linked adrenoleukodystrophy: Case report

RATIONALE: X-linked adrenoleukodystrophy (X-ALD) is the most common peroxisomal disorder, which is inherited as an X-linked recessive trait. ATP binding cassette subfamily D member 1 (ABCD1) localized to Xq28 is the only gene associated with ALD. PATIENT CONCERNS: We report a case of Chinese boy wit...

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Detalles Bibliográficos
Autores principales: Wang, Jing, Zhu, Qian, Liu, Hongqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392892/
https://www.ncbi.nlm.nih.gov/pubmed/29794777
http://dx.doi.org/10.1097/MD.0000000000010837

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392892/
https://www.ncbi.nlm.nih.gov/pubmed/29794777
http://dx.doi.org/10.1097/MD.0000000000010837

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