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Paper Report for: Baass_2009_Atherosclerosis_207_452

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Title: Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype
Baass A, Wassef H, Tremblay M, Bernier L, Dufour R, Davignon J
Ref: Atherosclerosis, 207:452, 2009 : PubMed

        



Related information

Mutation | H35fsX61_human-LCAT,



Citations formats

Baass A, Wassef H, Tremblay M, Bernier L, Dufour R, Davignon J (2009)
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype
Atherosclerosis 207: 452-7

Baass A, Wassef H, Tremblay M, Bernier L, Dufour R, Davignon J (2009)
Atherosclerosis 207: 452-7



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