PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease. [electronic resource]
Producer: 20021029Description: 706-14 p. digitalISSN:- 0031-3998
- ATPases Associated with Diverse Cellular Activities
- Adolescent
- Adult
- Child
- Child, Preschool
- Fatty Acids -- blood
- Genetic Complementation Test
- Genotype
- Haplotypes
- Humans
- Membrane Proteins -- genetics
- Phenotype
- Polymorphism, Single-Stranded Conformational
- Severity of Illness Index
- Zellweger Syndrome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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