Monozygotic twins with X-linked adrenoleukodystrophy and different phenotypes [4]

Annals of Neurology

Volumn 50, Issue 3, 2001, Pages 424-

  Di Rocco, Maja ^a   Doria Lamba, Laura ^a   Caruso, Ubaldo ^a  

^a UNIVERSITY OF GENOA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

HLA DR ANTIGEN; MITOCHONDRIAL DNA; VERY LONG CHAIN FATTY ACID;

ADOLESCENT; ADRENOLEUKODYSTROPHY; CASE REPORT; DEMYELINATION; FATTY ACID OXIDATION; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; LETTER; MALE; MONOZYGOTIC TWINS; NERVE FIBER DEGENERATION; PEROXISOME; PHENOTYPE; PRIORITY JOURNAL; WHITE MATTER; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADRENOLEUKODYSTROPHY; HUMANS; MALE; PHENOTYPE; TWINS, MONOZYGOTIC;

EID: 0034842044     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1220     Document Type: Letter

References (5)

1. Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy
2. Targeted inactivation of the X-linked adrenoleukodystrophy in mice
3. Phenotypic heterogeneity of an adult form of adrenoleukodystrophy in monozygotic twins
4. Cerebral adrenoleukodystrophy (ADL) in only one of monozygous twins with an identical ADL genotype
5. Identical mitochondrial DNA in monozygotic twins with discordant adrenoleukodystrophy phenotype