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Search Results - Meyer-Kleine, C
Search Results - Meyer-Kleine, C
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Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia
by
MEYER-KLEINE, C
,
STEINMEYER, K
,
RICKER, K
,
JENTSCH, T. J
,
KOCH, M. C
Published in
American journal of human genetics
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Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia
by
Lorenz, Claudius
,
Meyer-Kleine, Christof
,
Steinmeyer, Klaus
,
Koch, Manuela C.
,
Jentsch, Thomas J.
Published in
Human molecular genetics
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A recurrent 14 bp deletion in the CLCN1 gene associated with generalized myotonia (Becker)
by
Meyer-Kleine, Christof
,
Ricker, Kenneth
,
Otto, Michael
,
Koch, Manuela C.
Published in
Human molecular genetics
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Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families
by
MEYER-KLEIN, C
,
OTTO, M
,
ZOLL, B
,
KOCH, M. C
Published in
Human genetics
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Double-blind, randomized feedback control fails to improve the hypocholestrolemic effect of a plant-based low-fat diet in patients with moderately elevated total cholesterol levels
by
Koebnick, C
,
Plank-Habibi, S
,
Wirsam, B
,
Gruendel, S
,
Hahan, A
,
Meyer-Kleine, C
,
Leitzmann, C
,
Zunft, H.J.F
Published in
European journal of clinical nutrition
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Double-blind, randomized feedback control fails to improve the hypocholesterolemic effect of a plant-based low-fat diet in patients with moderately elevated total cholesterol level...
by
Koebnick, C
,
Plank-Habibi, S
,
Wirsam, B
,
Gruendel, S
,
Hahn, A
,
Meyer-Kleine, C
,
Leitzmann, C
,
Zunft, H J F
Published in
European journal of clinical nutrition
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A recurrent 14bp deletion in the CLCN1 gene associated with generalized myotonia (Becker)
by
MEYER-KLEINE, C
,
RICKER, K
,
OTTO, M
,
KOCH, M. C
Published in
Human molecular genetics
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