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Paper Report for: Evans_1998_Hum.Mutat_12_217

Reference

Title: Compound heterozygosity for a new (S259G) and a previously described (G188E) mutation in lipoprotein lipase (LpL) as a cause of chylomicronemia. Mutations in brief no. 183. Online
Evans D, Wendt D, Ahle S, Guerra A, Beisiegel U
Ref: Hum Mutat, 12:217, 1998 : PubMed

        



Related information

Gene_Locus| human-LPL
Mutation | S286G_human-LPL, G215E_human-LPL,



Citations formats

Evans D, Wendt D, Ahle S, Guerra A, Beisiegel U (1998)
Compound heterozygosity for a new (S259G) and a previously described (G188E) mutation in lipoprotein lipase (LpL) as a cause of chylomicronemia. Mutations in brief no. 183. Online
Hum Mutat 12: 217

Evans D, Wendt D, Ahle S, Guerra A, Beisiegel U (1998)
Hum Mutat 12: 217



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