(Q28263895)

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1516702

4 October 2022

J. P. Blomhoff

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1516702

4 October 2022

J. Solheim

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1516702

4 October 2022

H. Prydz

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1516702

Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression

4 October 2022

language of work or name

English

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publication date

14 September 1992

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published in

FEBS Letters

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volume

309

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issue

3

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page(s)

307-10

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cites work

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

An amino acid exchange in exon I of the human lecithin: cholesterol acyltransferase (LCAT) gene is associated with fish eye disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

Genetics of LCAT (lecithin: cholesterol acyltransferase) deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

The isolation and characterisation of a cDNA clone for human lecithin:cholesterol acyl transferase and its use to analyse the genes in patients with LCAT deficiency and fish eye disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: physical and chemical studies of low and high density lipoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

Differential phenotypic expression by three mutant alleles in familial lecithin:cholesterol acyltransferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

Lecithin-cholesterol acyltransferase (LCAT) deficiency with a missense mutation in exon 6 of the LCAT gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

Familial lecithin-cholesterol acyltransferase deficiency in four Norwegian Families. Evidence for low levels of a functionally defective enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2892%2980795-I

10.1016/0014-5793(92)80795-I

21 January 2018

Identifiers

DOI

0 references