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Year | Number of Results |
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1992 | 1 |
1993 | 1 |
1994 | 1 |
2025 | 0 |
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Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
Nat Genet. 1993 Apr;3(4):305-10. doi: 10.1038/ng0493-305.
Nat Genet. 1993.
PMID: 7981750
The skeletal muscle chloride channel in dominant and recessive human myotonia.
Koch MC, Steinmeyer K, Lorenz C, Ricker K, Wolf F, Otto M, Zoll B, Lehmann-Horn F, Grzeschik KH, Jentsch TJ.
Koch MC, et al.
Science. 1992 Aug 7;257(5071):797-800. doi: 10.1126/science.1379744.
Science. 1992.
PMID: 1379744
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Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia.
Lorenz C, Meyer-Kleine C, Steinmeyer K, Koch MC, Jentsch TJ.
Lorenz C, et al.
Hum Mol Genet. 1994 Jun;3(6):941-6. doi: 10.1093/hmg/3.6.941.
Hum Mol Genet. 1994.
PMID: 7951242
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