Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders. [electronic resource]
Producer: 20090528Description: E467-80 p. digitalISSN:- 1098-1004
- ATPases Associated with Diverse Cellular Activities
- Adenosine Triphosphatases -- genetics
- Alleles
- Cell Fusion
- Cohort Studies
- DNA Mutational Analysis
- Fibroblasts -- metabolism
- Gene Frequency
- Genetic Complementation Test -- methods
- Genetic Predisposition to Disease
- Genotype
- Humans
- Membrane Proteins -- genetics
- Mutation
- Peroxins
- Peroxisomal Disorders -- genetics
- Peroxisomes -- metabolism
- Receptors, Cytoplasmic and Nuclear -- genetics
- Zellweger Syndrome -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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