(Q41503170)

1 October 2017

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries (English)

1 reference

1 October 2017

Ma Y

1

1 reference

1 October 2017

Liu MS

2

1 reference

1 October 2017

Chitayat D

3

1 reference

1 October 2017

Bruin T

4

1 reference

1 October 2017

Beisiegel U

5

1 reference

1 October 2017

Benlian P

6

1 reference

1 October 2017

Foubert L

7

1 reference

1 October 2017

De Gennes JL

8

1 reference

1 October 2017

Funke H

9

1 reference

1 October 2017

Forsythe I

10

1 reference

1 October 2017

1 January 1994

1 reference

1 October 2017

1 reference

1 October 2017

3

1 reference

1 October 2017

1

1 reference

1 October 2017

52-58

1 reference

Detection and characterization of the heterozygote state for lipoprotein lipase deficiency

1 October 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Evolution of the genome and the genetic code: selection at the dinucleotide level by methylation and polyribonucleotide cleavage

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

DNA restriction fragment length polymorphisms and heterozygosity in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Diagnosis of genetic disease using recombinant DNA. Second edition

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Two polymorphisms in the human lipoprotein lipase (LPL) gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Hind III RFLP in the lipoprotein lipase gene, (LPL).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Molecular genetics of human lipoprotein lipase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric origin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172-->Cys mutation in the lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Tetranucleotide repeat polymorphism in the LPL gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030109

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380030109

1 reference

1 October 2017

1 reference