Multiple genotypes, multiple phenotypes, and partial defects. [electronic resource]
Producer: 19810723Description: 31-40 p. digitalISSN:- 0148-639X
- Anemia, Hemolytic, Congenital -- genetics
- Arylsulfatases -- deficiency
- Female
- Genetic Variation
- Genotype
- Glucosephosphate Dehydrogenase Deficiency -- genetics
- Glycogen Storage Disease Type V -- genetics
- Humans
- Hyperlipoproteinemia Type II -- genetics
- Male
- Models, Genetic
- Muscular Atrophy -- genetics
- Neuromuscular Diseases -- genetics
- Phenotype
- Porphyrias -- genetics
- Pyruvate Kinase -- deficiency
- Tay-Sachs Disease -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
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