(Q51561106)

English

Identification of compound heterozygous mutations (G188E/W382X) of lipoprotein lipase gene in a Japanese infant with hyperchylomicronemia: the G188E mutation was newly identified in Japanese.

scientific article published in July 1999

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scholarly article

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

Identification of compound heterozygous mutations (G188E/W382X) of lipoprotein lipase gene in a Japanese infant with hyperchylomicronemia: the G188E mutation was newly identified in Japanese. (English)

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

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author name string

A Takagi

1

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

Y Ikeda

2

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

K Tachi

3

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

T Shinozuka

4

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

A Yamamoto

5

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

publication date

1 July 1999

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

Clinica Chimica Acta

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

285

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

1-2

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

143-154

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

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/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Purification and characterization of lipoprotein lipase and hepatic triglyceride lipase from human postheparin plasma: production of monospecific antibody to the individual lipase

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Development of a direct DNA sequencing method for detecting heterozygous mutations of the human lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Human lipoprotein lipase complementary DNA sequence.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Two polymorphisms in the human lipoprotein lipase (LPL) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Molecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

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/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Identification of homozygous lipoprotein lipase gene mutation in a woman with recurrent aggravation of hypertriglyceridaemia induced by pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2899%2900116-3

7 January 2021

Identifiers

10.1016/S0009-8981(99)00116-3

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/10481930

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