TY  - GEN
AU  - McLean,B N
AU  - Allen,J
AU  - Ferdinandusse,S
AU  - Wanders,R J A
TI  - A new defect of peroxisomal function involving pristanic acid: a case report
SN  - 0022-3050
PY  - 2002///0328
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Chromosome Aberrations
KW  - Fatty Acids
KW  - blood
KW  - Genes, Recessive
KW  - genetics
KW  - Humans
KW  - Learning Disabilities
KW  - Male
KW  - Middle Aged
KW  - Peroxisomal Disorders
KW  - Racemases and Epimerases
KW  - deficiency
KW  - Retinitis Pigmentosa
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1136/jnnp.72.3.396
ER  -