Identification of a double mutation in the low‐density lipoprotein receptor gene causing familial hypercholesterolemia
- 1 December 1996
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 50 (6) , 525-526
- https://doi.org/10.1111/j.1399-0004.1996.tb02727.x
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Mutations in the low density lipoprotein receptor gene of familial hypercholesterolemic patients detected by denaturing gradient gel electrophoresis and direct sequencing.Journal of Lipid Research, 1995
- Identification of a mutation, N543H, in exon 11 of the low-density lipoprotein receptor gene in a French family with familial hypercholesterolemiaHuman Mutation, 1995
- Molecular genetics of the LDL receptor gene in familial hypercholesterolemiaHuman Mutation, 1992
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- The human LDL receptor: A cysteine-rich protein with multiple Alu sequences in its mRNACell, 1984