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This Concept Map, created with IHMC CmapTools, has information related to: Myotonic Dystrophy - final CMAP, Miriam Husband, Miriam Dressner Presents with Mild bilateral ptosis, abnormal function of genes including skeletal muscle chloride channel, autosomal dominant condition explaining brother affected, Miriam Dressner Presents with Facial Weakness, heart problems seen in family history of multiple members with MIs, Na+ causes action potential, CUG RNA expansion is mutant RNA, MI in Paternal grandmother, Miriam Dressner has family history of Mother with dysphagia, 0/4 for patellar and achilles may indicate nerve damage, relaxation of muscle fiber, Miriam Daughter, expansion of CTG nucleotide on chromosome 19q 13.3, Miriam Dressner Presents with Mild Dyspnea, same generation exhibit varying severity of phenotypes, MBNL which is an RNA-binding protein, Miriam Dressner Has history of Cataract Repair, myosin binding sites on actin, removal of muscle tissue shows severely Atrophied Muscle Fibers