Associated Papers
Ocular findings and genomics of X-linked recessive disorders: A review.
Hassan A et al.
Indian Journal of Ophthalmology, 2022
Novel ABCD1 Gene Mutation in a Korean Patient with X-Linked Adrenoleukodystrophy Presenting with Addison's Disease.
Cho YK et al.
Endocrinology and Metabolism (seoul, Korea), 2020
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms.
Salsano E et al.
Orphanet Journal of Rare Diseases, 2012
Select a paper to view details