Publication | Open Access

Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders

Adrenal GlandMendelian DisorderX-linked Adrenoleukodystrophy GeneGenetic DisorderGeneticsInherited Metabolic DiseasePathologyContiguous DeletionDegenerative DiseasePeroxisomal Biogenesis DisordersMedicine