000 01137 a2200337 4500
005 20250513185653.0
264 0 _c19990916
008 199909s 0 0 eng d
022 _a0021-9150
024 7 _a10.1016/s0021-9150(99)00096-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKotze, M J
245 0 0 _aMedped FH: a paradigm for other common monogenic diseases in South Africa.
_h[electronic resource]
260 _bAtherosclerosis
_cJun 1999
300 _a467-8 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChild
650 0 4 _aChromosome Aberrations
_xgenetics
650 0 4 _aChromosome Disorders
650 0 4 _aGenes, Dominant
_xgenetics
650 0 4 _aGenetic Carrier Screening
650 0 4 _aGenetics, Population
650 0 4 _aHumans
650 0 4 _aHyperlipoproteinemia Type II
_xgenetics
650 0 4 _aMutation
_xgenetics
650 0 4 _aReceptors, LDL
_xgenetics
650 0 4 _aSouth Africa
700 1 _aCallis, M
773 0 _tAtherosclerosis
_gvol. 144
_gno. 2
_gp. 467-8
856 4 0 _uhttps://doi.org/10.1016/s0021-9150(99)00096-9
_zAvailable from publisher's website
999 _c10365621
_d10365621