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Q24678433-C2D4FBDA-A982-442F-ABA2-A7339DE3320C
Q24678433-C2D4FBDA-A982-442F-ABA2-A7339DE3320C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24678433-C2D4FBDA-A982-442F-ABA2-A7339DE3320C
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene
P2860
Q24678433-C2D4FBDA-A982-442F-ABA2-A7339DE3320C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24678433-C2D4FBDA-A982-442F-ABA2-A7339DE3320C
rank
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type
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wasDerivedFrom
153a18e80b902603864206aaf0e2ce6f1ea50157
P2860
Nucleotide sequence of human liver carbonic anhydrase II cDNA