Summary Report for: Natural mutation; Silent phenotype;Primo-Parmo_1992_4th.ChE.Meeting.Eilat__61;Primo-Parmo_1996_Am.J.Hum.Genet_58_52
Natural mutation; Silent phenotype;Primo-Parmo_1992_4th.ChE.Meeting.Eilat__61;Primo-Parmo_1996_Am.J.Hum.Genet_58_52 | Mutation | S198G_human-BCHE |
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