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Q33844920-B22F9CA1-76B3-44B6-8D5A-BD012EB34DF8
Q33844920-B22F9CA1-76B3-44B6-8D5A-BD012EB34DF8
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http://www.wikidata.org/entity/statement/Q33844920-B22F9CA1-76B3-44B6-8D5A-BD012EB34DF8
Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease as
P2860
Q33844920-B22F9CA1-76B3-44B6-8D5A-BD012EB34DF8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33844920-B22F9CA1-76B3-44B6-8D5A-BD012EB34DF8
rank
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wasDerivedFrom
f8bdc787f3c24248054ef18aac0920f81b02af22
P2860
Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.