PMC:1584416 / 457-726
Annnotations
craft-sa-dev
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craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T26","span":{"begin":11,"end":18},"obj":"SO:0000704"},{"id":"T27","span":{"begin":81,"end":88},"obj":"SO:0001023"},{"id":"T28","span":{"begin":147,"end":150},"obj":"PR:000007164"},{"id":"T29","span":{"begin":196,"end":201},"obj":"NCBITaxon:10088"}],"text":"ronment or genetic background. We addressed the potential of different recessive alleles to contribute to the enigmatic pleiotropy associated with XPD recessive disorders in compound heterozygous mouse models. Alterations in this essential helicase, with functions in b"}
craft-ca-core-ex-dev
{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T56","span":{"begin":11,"end":18},"obj":"SO_EXT:0000704"},{"id":"T57","span":{"begin":81,"end":88},"obj":"SO_EXT:0001023"},{"id":"T58","span":{"begin":147,"end":150},"obj":"PR_EXT:000007164"},{"id":"T59","span":{"begin":196,"end":201},"obj":"NCBITaxon:10088"},{"id":"T60","span":{"begin":210,"end":221},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T61","span":{"begin":240,"end":248},"obj":"GO_EXT:0004386"}],"text":"ronment or genetic background. We addressed the potential of different recessive alleles to contribute to the enigmatic pleiotropy associated with XPD recessive disorders in compound heterozygous mouse models. Alterations in this essential helicase, with functions in b"}