Disorders of peroxisome biogenesis: Complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)
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| Veröffentlicht in: | Journal of inherited metabolic disease 1999-05, Vol.22 (3), p.314-318 |
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| container_end_page | 318 |
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| container_issue | 3 |
| container_start_page | 314 |
| container_title | Journal of inherited metabolic disease |
| container_volume | 22 |
| creator | Wanders, R. J. A. Mooijer, P. A. W. Dekker, C. Suzuki, Y. Shimozawa, N. |
| description | |
| doi_str_mv | 10.1023/A:1005504104541 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0141-8955 |
| ispartof | Journal of inherited metabolic disease, 1999-05, Vol.22 (3), p.314-318 |
| issn | 0141-8955 1573-2665 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_69856943 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete; SpringerLink Journals |
| subjects | ATPases Associated with Diverse Cellular Activities Biological and medical sciences Catalase - analysis Errors of metabolism Genetic Complementation Test Genetic Heterogeneity Humans Lipids (lysosomal enzyme disorders, storage diseases) Medical sciences Membrane Proteins - genetics Metabolic diseases Microbodies Microscopy, Fluorescence Peroxisomal Disorders - genetics Zellweger Syndrome - genetics |
| title | Disorders of peroxisome biogenesis: Complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency) |
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