ABCD1 Dysfunction Alters White Matter Microvascular PerfusionLauer, ArneBrain2017DOI 10.1093/brain/awx262
ABCD1 Transporter Deficiency Results in Altered Cholesterol HomeostasisAgnieszka BudaMDPI AG2023DOI 10.3390/biom13091333
Downregulation of ABCD1 in Human Renal Cell CarcinomaHour, Tzyh-ChyuanSAGE Publications2009DOI 10.1177/172460080902400307
ABCD1 Gene Mutations in Chinese Patients With X-Linked AdrenoleukodystrophyHong PanPediatric Neurology2005DOI 10.1016/j.pediatrneurol.2005.03.006
ABCD1 Translation-initiator Mutation Demonstrates Genotype-phenotype Correlation for AMNO'Neill, G. N.Lippincott Williams and Wilkins2001DOI 10.1212/wnl.57.11.1956
Targeted Gene Approach with Biochemical Assay Confirms ABCD1 MutationMauermann, Michelle L.Neuromuscular Disorders2018DOI 10.1016/j.nmd.2018.11.007
X-linked Adrenoleukodystrophy: ABCD1 De Novo Mutations and MosaicismYing WangMolecular Genetics and Metabolism2011DOI 10.1016/j.ymgme.2011.05.016
Spinocerebellar Variant of Adrenoleukodystrophy with a Novel ABCD1 Gene MutationJie-Yuan LiElsevier Science2010DOI 10.1016/j.jns.2009.12.002
Étude moléculaire du gène ABCD1 chez 4 familles tunisiennes atteintes d’adrénoleucodystrophieKallabi, F.Annales d Endocrinologie2013DOI 10.1016/j.ando.2013.07.354
A Novel Mutation of the ABCD1 Gene in Serbian X-AdrenoleukodystrophyGrkovic, SVersita2008DOI 10.2478/v10034-008-0020-2
Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 MutationBenzoni, ChiaraLippincott Williams and Wilkins2019DOI 10.1097/nrl.0000000000000252
Role of ALDP (ABCD1) and Mitochondria in X-Linked AdrenoleukodystrophyMcGuinness, M. C.American Society for Microbiology2003DOI 10.1128/mcb.23.2.744-753.2003
