01309nam a2200289Ia 4500001000700000003000600007005001700013008004100030015001900071020001800090020001500108035002100123040004600144050002200190082001500212082001500227245006500242260004600307300002800353490003900381504005100420505043900471650002500910650003100935700002500966700002800991289244OCoLC20160527201943.0080721s2008    ne a     b    001 0 eng d  aGBA8A49112bnb  a9780123745279  a0123745276  a(OCoLC)234450069  aBTCTAcBTCTAdBAKERdYDXCPdTHMdMTGdUKM 4aQH431.A1bA3 V.6304a571.6422204a616.0722200aIon channel diseasescedited by Guy Rouleau, Claudia Gaspar.  aAmsterdamaBostonbAcademic Presscc2008.  ax, 157 p.bill.c24 cm. 0aAdvances in geneticsvv. 632Local  aIncludes bibliographical references and index.00tPeriodic paralysisrBertrand Fontaine --tMyotonia congenitarChristoph Lossin and Alfred L. George, Jr. --tFamilial hemiplegic migrainerCurtis F. Barrett ... [et al.] --tGenetics and molecular pathophysiology of Na [v below line] 1.7-related pain syndromesrSulayman D. Dib-Hajj, Yong Yang, and Stephen G. Waxman --tChannelopathies of transepithelial transport and vesicular functionrChristian A. Hübner and Thomas J. Jentsch. 0aIon channels.2Local 0aMembrane disorders.2Local1 aRouleau, Guy.2Local1 aGaspar, Claudia.2Local