PMC:1584416 / 72-282 JSONTXT

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{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/1584416","sourcedb":"PMC","sourceid":"1584416","source_url":"http://www.ncbi.nlm.nih.gov/pmc/1584416","text":"es\nCompound Heterozygosity at theXpd Locus\n\nAbstract\nAlthough compound heterozygosity, or the presence of two different mutant alleles of the same gene, is common in human recessive disease, its potential to 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