Molecular analysis of peroxisomal β-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect
Samia Guerroui, Patrick Aubourg, Winston W. Chen, Takashi Hashimoto, Jacques ScottoVolume:
161
Year:
1989
Language:
english
Pages:
252
DOI:
10.1016/0006-291x(89)91587-8
File:
PDF, 1.33 MB
english, 1989