000			02110cam a2200433La 4500
001			ocn646803053
003			OCoLC
005			20141103172210.0
006			m o u
007			cr cn|||||||||
008			080721s2008 ne a ob 001 0 eng d
040			_aE7B _beng _cE7B _dOCLCQ _dOPELS _dOCLCQ _dOCLCF
020			_a9780123745279 (electronic bk.)
020			_a0123745276 (electronic bk.)
029	1		_aDEBSZ _b405330383
035			_a(OCoLC)646803053
050		4	_aQH431.A1 _bA363 2008eb
082	0	4	_a571.6/4 _223
049			_aTEFA
245	0	0	_aAdvances in genetics _h[electronic resource] . _nVolume 63, _pIon channel diseases / _cedited by Guy Rouleau, Claudia Gaspar.
246	3		_aIon channel diseases
260			_aAmsterdam ; _aBoston : _bAcademic Press, _cc2008.
300			_a1 online resource (x, 157 p.) : _bill.
490	0		_aAdvances in genetics ; _vv. 63
504			_aIncludes bibliographical references and index.
588			_aDescription based on print version record.
520			_aIon channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic component. This volume presents a broad and comprehensive overview of the inherited channelopathies in humans, including clinical, genetic and molecular aspects of these conditions, as well as novel genomic and modeling research approaches. Also included is a review of potential therapeutic approaches for each of these conditions.
650		0	_aIon channels.
650		0	_aMembrane disorders.
650		7	_aIon channels. _2fast _0(OCoLC)fst00978573
650		7	_aMembrane disorders. _2fast _0(OCoLC)fst01015838
655		4	_aElectronic books.
700	1		_aRouleau, Guy.
700	1		_aGaspar, Claudia, _cPh. D.
856	4	0	_3ScienceDirect _uhttp://www.sciencedirect.com/science/book/9780123745279
938			_aebrary _bEBRY _nebr10282334
942			_cEB
994			_aC0 _bTEF
999			_c20846 _d20846