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Q24618688-38B80B65-A38B-4194-B8BB-6AEB0E65CD4B
Q24618688-38B80B65-A38B-4194-B8BB-6AEB0E65CD4B
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Statement
http://www.wikidata.org/entity/statement/Q24618688-38B80B65-A38B-4194-B8BB-6AEB0E65CD4B
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association
P2860
Q24618688-38B80B65-A38B-4194-B8BB-6AEB0E65CD4B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24618688-38B80B65-A38B-4194-B8BB-6AEB0E65CD4B
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wasDerivedFrom
b1d4fec79799fae0b3a280346afe9743ccb3f9df
P2860
Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families.