Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype

Clinical Chemistry

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Bibliographic Details
Main Authors:	Choong, M.-L., Koay, E.S.C., Khoo, K.-L., Khaw, M.-C., Sethi, S.K.
Other Authors:	PATHOLOGY
Format:	Article
Published:	2014
Subjects:	Genetic screening Heritable disorders Population screening
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/113426
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Institution:	National University of Singapore

id	sg-nus-scholar.10635-113426
record_format	dspace
spelling	sg-nus-scholar.10635-1134262024-11-09T08:33:30Z Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype Choong, M.-L. Koay, E.S.C. Khoo, K.-L. Khaw, M.-C. Sethi, S.K. PATHOLOGY Genetic screening Heritable disorders Population screening Clinical Chemistry 43 6 916-923 CLCHA 2014-12-01T06:54:20Z 2014-12-01T06:54:20Z 1997 Article Choong, M.-L.,Koay, E.S.C.,Khoo, K.-L.,Khaw, M.-C.,Sethi, S.K. (1997). Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype. Clinical Chemistry 43 (6) : 916-923. ScholarBank@NUS Repository. 00099147 http://scholarbank.nus.edu.sg/handle/10635/113426 NOT_IN_WOS Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	Genetic screening Heritable disorders Population screening
spellingShingle	Genetic screening Heritable disorders Population screening Choong, M.-L. Koay, E.S.C. Khoo, K.-L. Khaw, M.-C. Sethi, S.K. Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
description	Clinical Chemistry
author2	PATHOLOGY
author_facet	PATHOLOGY Choong, M.-L. Koay, E.S.C. Khoo, K.-L. Khaw, M.-C. Sethi, S.K.
format	Article
author	Choong, M.-L. Koay, E.S.C. Khoo, K.-L. Khaw, M.-C. Sethi, S.K.
author_sort	Choong, M.-L.
title	Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
title_short	Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
title_full	Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
title_fullStr	Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
title_full_unstemmed	Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
title_sort	denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein b-100 in a mixed asian cohort: two cases of arginine3500 → tryptophan mutation associated with a unique haplotype
publishDate	2014
url	http://scholarbank.nus.edu.sg/handle/10635/113426
_version_	1821212124256403456

Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: Two cases of arginine3500 → tryptophan mutation associated with a unique haplotype

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