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Frontiers in Genetics
Jianjun Ma, Jinhua Zheng, Xiaoxue Shi
exaly  

Distal Xq28 microdeletions: Clarification of the spectrum of contiguous gene deletions involving ABCD1, BCAP31, and SLC6A8 with a new case and review of the literature

American Journal of Medical Genetics, Part A, 2014
Amy Calhoun
exaly  

Novel human pathological mutations. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.

Human genetics, 2009
Neeraj, Kumar, K K, Taneja, Veena, Kalra, Madhuri, Behari, S, Aneja, S K, Bansal   +5 more
openaire   +3 more sources

Molecular analysis of ABCD1 gene in moroccan patients with X-linked adrenoleukodystrophy

Clinica Chimica Acta
F.Z. Madani Benjelloun, Y. Kriouile, D. Cheillan, L. Chabraoui   +3 more
openaire   +1 more source