PMC:1584416 / 30160-30397 JSONTXT

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{"project":"craft-ca-core-dev","denotations":[{"id":"T5526","span":{"begin":124,"end":131},"obj":"SO:0001023"},{"id":"T5527","span":{"begin":144,"end":147},"obj":"PR:000007164"},{"id":"T5528","span":{"begin":200,"end":203},"obj":"PR:000007164"},{"id":"T5529","span":{"begin":230,"end":233},"obj":"PR:000007164"}],"text":"pothesis comes from a number of XP complementation group D patients that do not fit within the framework of the current monoallelic paradigm of XPD disorders (Figure 5). In contrast to two hemizygous XPDXPCS patients carrying the XPDG47R"}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T5572","span":{"begin":124,"end":131},"obj":"SO_EXT:0001023"},{"id":"T5573","span":{"begin":144,"end":147},"obj":"PR_EXT:000007164"},{"id":"T5574","span":{"begin":200,"end":203},"obj":"PR_EXT:000007164"},{"id":"T5575","span":{"begin":230,"end":233},"obj":"PR_EXT:000007164"}],"text":"pothesis comes from a number of XP complementation group D patients that do not fit within the framework of the current monoallelic paradigm of XPD disorders (Figure 5). In contrast to two hemizygous XPDXPCS patients carrying the XPDG47R"}