Authors: MEYERKLEINE C STEINMEYER K RICKER K JENTSCH TJ KOCH MC

Citation: C. Meyerkleine et al., SPECTRUM OF MUTATIONS IN THE MAJOR HUMAN SKELETAL-MUSCLE CHLORIDE CHANNEL GENE (CLCNUI) LEADING TO MYOTONIA, American journal of human genetics, 57(6), 1995, pp. 1325-1334

Authors: LORENZ C MEYERKLEINE C STEINMEYER K KOCH MC JENTSCH TJ

Citation: C. Lorenz et al., GENOMIC ORGANIZATION OF THE HUMAN MUSCLE CHLORIDE CHANNEL CIC-1 AND ANALYSIS OF NOVEL MUTATIONS LEADING TO BECKER-TYPE MYOTONIA, Human molecular genetics, 3(6), 1994, pp. 941-946

Authors: MEYERKLEINE C RICKER K OTTO M KOCH MC

Citation: C. Meyerkleine et al., A RECURRENT 14-BP DELETION IN THE CLCN1 GENE ASSOCIATED WITH GENERALIZED MYOTONIA (BECKER), Human molecular genetics, 3(6), 1994, pp. 1015-1016

Authors: MEYERKLEINE C OTTO M ZOLL B KOCH MC

Citation: C. Meyerkleine et al., MOLECULAR AND GENETIC-CHARACTERIZATION OF GERMAN FAMILIES WITH PARAMYOTONIA-CONGENITA AND DEMONSTRATION OF FOUNDER EFFECT IN THE RAVENSBERGFAMILIES, Human genetics, 93(6), 1994, pp. 707-710

Authors: KOCH MC STEINMEYER K OTTO M LORENZ C MEYERKLEINE C RICKER K JENTSCH TJ

Citation: Mc. Koch et al., MAPPING AND CHARACTERIZATION OF THE GENE FOR HUMAN MYOTONIA, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 71-71