Functional characterization of ClC-1 mutations from patients affected by recessive myotonia congenita presenting with different clinical phenotypes. Desaphy JF, Gramegna G, Altamura C, Dinardo MM, Imbrici P, George AL, Modoni A, Lomonaco M, Conte Camerino D (2013) Exp Neurol 248: 530-40 Myotonia congenita. A histochemical and ultrastructural study in the goat: comparison with abnormalities found in human myotonia dystrophica. Atkinson JB, Swift LL, Lequire VS (1981) Am J Pathol 102: 324-35 Electron paramagnetic resonance and saturation transfer electron paramagnetic resonance studies on erythrocytes from goats with and without heritable myotonia. Swift LL, Atkinson JB, Perkins RC, Dalton LR, LeQuire VS (1980) J Membr Biol 52: 165-72 SAR inspired by aldehyde oxidase (AO) metabolism: Discovery of novel, CNS penetrant tricyclic M PAMs. Chopko TC, Han C, Gregro AR, Engers DW, Felts AS, Poslusney MS, Bollinger KA, Morrison RD, Bubser M, Lamsal A, Luscombe VB, Cho HP, Schnetz-Boutaud NC, Rodriguez AL, Chang S, Daniels JS, Stec DF, Niswender CM, Jones CK, Wood MR, Wood MW, Duggan ME, Brandon NJ, Conn PJ, Bridges TM, Lindsley CW, Melancon BJ (2019) Bioorg Med Chem Lett 29: 2224-2228
Hints: (1) double-click or double-tap to navigate to a node. (2) Grab a node and move it to arrange the graph.