TY  - GEN
AU  - Corzo,Deyanira
AU  - Gibson,William
AU  - Johnson,Kisha
AU  - Mitchell,Grant
AU  - LePage,Guy
AU  - Cox,Gerald F
AU  - Casey,Robin
AU  - Zeiss,Carolyn
AU  - Tyson,Heidi
AU  - Cutting,Garry R
AU  - Raymond,Gerald V
AU  - Smith,Kirby D
AU  - Watkins,Paul A
AU  - Moser,Ann B
AU  - Moser,Hugo W
AU  - Steinberg,Steven J
TI  - Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders
SN  - 0002-9297
PY  - 2002///0627
KW  - ATP Binding Cassette Transporter, Subfamily D, Member 1
KW  - ATP-Binding Cassette Transporters
KW  - genetics
KW  - Adrenoleukodystrophy
KW  - diagnosis
KW  - Age of Onset
KW  - Chemokine CCL22
KW  - Chemokines, CC
KW  - Child
KW  - Child, Preschool
KW  - Exons
KW  - Female
KW  - Fibroblasts
KW  - Genetic Complementation Test
KW  - Heterozygote
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Infant, Newborn, Diseases
KW  - Male
KW  - Membrane Proteins
KW  - deficiency
KW  - Peroxisomal Disorders
KW  - Peroxisomes
KW  - metabolism
KW  - Phenotype
KW  - Prenatal Diagnosis
KW  - Promoter Regions, Genetic
KW  - Proteins
KW  - Sequence Deletion
KW  - Syndrome
KW  - X Chromosome
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/340849
ER  -