(Q78004723)

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Detection of a new compound heterozygote (del G916/G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients

scientific article published on 01 June 1999

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407506%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Detection of a new compound heterozygote (del G916/G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407506%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

author name string

M Okubo

1

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10 December 2019

S Inoue

2

1 reference

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10 December 2019

A Horinishi

3

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10 December 2019

T Ogihara

4

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10 December 2019

K Kaneko

5

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10 December 2019

T Gotoda

6

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10 December 2019

N Yamada

7

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10 December 2019

T Murase

8

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10 December 2019

publication date

1 June 1999

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10 December 2019

Atherosclerosis

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10 December 2019

144

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10 December 2019

2

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10 December 2019

443-447

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10 December 2019

Plasma apolipoprotein CII levels in hypertriglyceridemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

7 January 2021

Decline of postheparin plasma lipoprotein lipase in acromegalic patients

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

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%2FS0021-9150%2899%2900008-8

7 January 2021

A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

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%2FS0021-9150%2899%2900008-8

7 January 2021

Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

7 January 2021

Dinucleotide repeat polymorphisms at the lipoprotein lipase (LPL) locus

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

7 January 2021

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

7 January 2021

A G+1 to C mutation in a donor splice site of intron 2 in the apolipoprotein (apo) C-II gene in a patient with apo C-II deficiency. A possible interaction between apo C-II deficiency and apo E4 in a severely hypertriglyceridemic patient.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900008-8

7 January 2021

Identifiers

10.1016/S0021-9150(99)00008-8

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10 December 2019

1 reference

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10 December 2019

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