M97820[Secondary Source ID] - Search 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).

George AL Jr, Crackower MA, Abdalla JA, Hudson AJ, Ebers GC. George AL Jr, et al. 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

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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