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CKMM |
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Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms. The specificity is indicated by the complete lack of inhibition of CKMM or CKBB (Fig. |
CKMM |
CKKP CKKS CKKT CKL CKLAG CKLC CKLEAC CKLG CKLKS CKLN CKLOM CKLRS CKLS CKLT CKLV CKLVI CKM CKM Instructor CKMB CKMC CKME CKMG CKMI CKML CKMM CKMNCCKMP CKMR CKMS CKMT CKMU CKN CKNAC CKND CknG CKNJ CKNM CKNN CKNS CKNY CKO CKO CKOA Ckockroach Ckockroach Ckockroach Ckockroch Ckockroch Ckockroch Ckocroach Ckocroach Ckocroach Ckocroch Ckocroch Ckocroch | |||||
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