000			01818 a2200565 4500
005			20250514020731.0
264		0	_c20020307
008			200203s 0 0 eng d
022			_a1468-6244
024	7		_a10.1136/jmg.38.12.e43 _2doi
040			_aNLM _beng _cNLM
100	1		_aAndersen, P S
245	0	0	_aMyosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations. _h[electronic resource]
260			_bJournal of medical genetics _cDec 2001
300			_aE43 p. _bdigital
500			_aPublication Type: Letter; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aAged
650	0	4	_aCardiomyopathy, Hypertrophic _xepidemiology
650	0	4	_aDNA Mutational Analysis
650	0	4	_aEchocardiography
650	0	4	_aExons _xgenetics
650	0	4	_aFemale
650	0	4	_aGene Frequency _xgenetics
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aMutation _xgenetics
650	0	4	_aMutation, Missense _xgenetics
650	0	4	_aMyosin Light Chains _xgenetics
650	0	4	_aNetherlands _xepidemiology
650	0	4	_aPedigree
650	0	4	_aPhenotype
650	0	4	_aPolymorphism, Single-Stranded Conformational
650	0	4	_aSouth Africa _xepidemiology
700	1		_aHavndrup, O
700	1		_aBundgaard, H
700	1		_aMoolman-Smook, J C
700	1		_aLarsen, L A
700	1		_aMogensen, J
700	1		_aBrink, P A
700	1		_aBørglum, A D
700	1		_aCorfield, V A
700	1		_aKjeldsen, K
700	1		_aVuust, J
700	1		_aChristiansen, M
773	0		_tJournal of medical genetics _gvol. 38 _gno. 12 _gp. E43
856	4	0	_uhttps://doi.org/10.1136/jmg.38.12.e43 _zAvailable from publisher's website
999			_c11661109 _d11661109