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Q33676915-56B57FB7-07BE-4912-A20C-376F38DD19E4
Q33676915-56B57FB7-07BE-4912-A20C-376F38DD19E4
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http://www.wikidata.org/entity/statement/Q33676915-56B57FB7-07BE-4912-A20C-376F38DD19E4
C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.
P2860
Q33676915-56B57FB7-07BE-4912-A20C-376F38DD19E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33676915-56B57FB7-07BE-4912-A20C-376F38DD19E4
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wasDerivedFrom
2cfbbe95f88c39b76dd644967aaa1950772148de
P2860
The structural basis of the multiple forms of human complement component C4.