141 related articles for article (PubMed ID: 2570020)
1. Multiple mutations underlying familial hypercholesterolemia in the South African population.
Henderson HE; Kotze MJ; Berger GM
Hum Genet; 1989 Aug; 83(1):67-70. PubMed ID: 2570020
[TBL] [Abstract][Full Text] [Related]
2. South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population.
Defesche JC; van Diermen DE; Lansberg PJ; Lamping RJ; Reymer PW; Hayden MR; Kastelein JJ
Hum Genet; 1993 Dec; 92(6):567-70. PubMed ID: 7903269
[TBL] [Abstract][Full Text] [Related]
3. Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.
Miserez AR; Schuster H; Chiodetti N; Keller U
Am J Hum Genet; 1993 Apr; 52(4):808-26. PubMed ID: 8096361
[TBL] [Abstract][Full Text] [Related]
4. Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effect.
Brink PA; Steyn LT; Coetzee GA; Van der Westhuyzen DR
Hum Genet; 1987 Sep; 77(1):32-5. PubMed ID: 2887506
[TBL] [Abstract][Full Text] [Related]
5. Identification of two new LDL-receptor mutations causing homozygous familial hypercholesterolemia in a South African of Indian origin.
Rubinsztein DC; Jialal I; Leitersdorf E; Coetzee GA; van der Westhuyzen DR
Biochim Biophys Acta; 1993 Aug; 1182(1):75-82. PubMed ID: 8347689
[TBL] [Abstract][Full Text] [Related]
6. Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners.
Leitersdorf E; Van der Westhuyzen DR; Coetzee GA; Hobbs HH
J Clin Invest; 1989 Sep; 84(3):954-61. PubMed ID: 2569482
[TBL] [Abstract][Full Text] [Related]
7. Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry.
Loubser O; Marais AD; Kotze MJ; Godenir N; Thiart R; Scholtz CL; de Villiers JN; Hillermann R; Firth JC; Weich HF; Maritz F; Jones S; van der Westhuyzen DR
Clin Genet; 1999 May; 55(5):340-5. PubMed ID: 10422804
[TBL] [Abstract][Full Text] [Related]
8. Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.
Kotze MJ; Langenhoven E; Retief AE; Seftel HC; Henderson HE; Weich HF
J Med Genet; 1989 Apr; 26(4):255-9. PubMed ID: 2565980
[TBL] [Abstract][Full Text] [Related]
9. Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia.
Schuster H; Stiefenhofer B; Wolfram G; Keller C; Humphries S; Huber A; Zöllner N
Hum Genet; 1989 Apr; 82(1):69-72. PubMed ID: 2565869
[TBL] [Abstract][Full Text] [Related]
10. Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians.
Bétard C; Kessling AM; Roy M; Chamberland A; Lussier-Cacan S; Davignon J
Hum Genet; 1992 Mar; 88(5):529-36. PubMed ID: 1348044
[TBL] [Abstract][Full Text] [Related]
11. Recurrent LDL-receptor mutation causes familial hypercholesterolaemia in South African coloureds and Afrikaners.
Kotze MJ; Langenhoven E; Theart L; Loubser O; Micklem A; Oosthuizen CJ
S Afr Med J; 1995 May; 85(5):357-61. PubMed ID: 7638684
[TBL] [Abstract][Full Text] [Related]
12. An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics.
Kotze MJ; Warnich L; Langenhoven E; du Plessis L; Retief AE
J Med Genet; 1990 May; 27(5):298-302. PubMed ID: 2352257
[TBL] [Abstract][Full Text] [Related]
13. Low-density lipoprotein-receptor gene haplotypes in Afrikaans-speaking patients with homozygous familial hypercholesterolaemia. Further evidence in support of a founder gene.
Henderson HE; Landon SV; Berger GM
S Afr Med J; 1987 Feb; 71(4):218-20. PubMed ID: 3824088
[TBL] [Abstract][Full Text] [Related]
14. Monogenic primary hypercholesterolaemia in South Africa.
Rubinsztein DC; van der Westhuyzen DR; Coetzee GA
S Afr Med J; 1994 Jun; 84(6):339-44. PubMed ID: 7740380
[TBL] [Abstract][Full Text] [Related]
15. Use of three DNA polymorphisms of the LDL receptor gene in the diagnosis of familial hypercholesterolemia.
Daga A; Mattioni T; Balestreri R; Coviello DA; Corte G; Bertolini S
Hum Genet; 1990 Apr; 84(5):412-6. PubMed ID: 1969842
[TBL] [Abstract][Full Text] [Related]
16. A LDL receptor gene homozygous mutation: PCR amplification, direct genomic sequencing, associated haplotype, rapid screening for frequency.
Benlian P; Amselem S; Loux N; Pastier D; Giraud G; de Gennes JL; Turpin G; Monnier L; Rieu D; Douste-Blazy P
Ann Genet; 1990; 33(2):65-9. PubMed ID: 1978630
[TBL] [Abstract][Full Text] [Related]
17. TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.
Yamakawa K; Okafuji T; Iwamura Y; Yuzawa K; Satoh J; Hattori N; Yamanouchi Y; Yanagi H; Kawai K; Tsuchiya S
Hum Genet; 1988 Sep; 80(1):1-5. PubMed ID: 2901393
[TBL] [Abstract][Full Text] [Related]
18. Identification of the serine-156 to leucine mutation in the low-density lipoprotein receptor in a German family with familial hypercholesterolemia.
Schuster H; Ostwald P; Keller P; Wolfram G; Keller C
Clin Investig; 1993 Feb; 71(2):172-5. PubMed ID: 8096412
[TBL] [Abstract][Full Text] [Related]
19. Identification of a 76-year-old patient with compound heterozygous familial hypercholesterolemia by haplotype analysis of the LDL receptor gene.
Fischer HJ; Schuster H; Keller C; Wolfram G; Zöllner N
Klin Wochenschr; 1991 Nov; 69(18):842-6. PubMed ID: 1685207
[TBL] [Abstract][Full Text] [Related]
20. Seven DNA polymorphisms in the LDL receptor gene: application to the study of familial hypercholesterolemia in Spain.
Chaves FJ; Puig O; García-Sogo M; Real J; Gil JV; Ascaso J; Carmena R; Armengod ME
Clin Genet; 1996 Jul; 50(1):28-35. PubMed ID: 8891383
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]