Hypoalphalipoproteinemia resembling fish eye disease

scientific article published on 01 January 1987

Hypoalphalipoproteinemia resembling fish eye disease is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.0954-6820.1987.TB00896.X
P698PubMed publication ID3591467

P2093author name stringP H Pritchard
R McLeod
J Frohlich
M Hayden
L D Wadsworth
G Hoag
D V Godin
J D Critchley
P433issue3
P921main subjecteye diseaseQ3041498
hypoalphalipoproteinemiaQ5959167
P304page(s)291-298
P577publication date1987-01-01
P1433published inActa medica ScandinavicaQ10400528
P1476titleHypoalphalipoproteinemia resembling fish eye disease
P478volume221

Reverse relations

cites work (P2860)
Q39607928A first British case of fish-eye disease presenting at age 75 years: a double heterozygote for defined and new mutations affecting LCAT structure and expression
Q33382898A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities
Q24561532A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity
Q47655146A retractable lid in lecithin:cholesterol acyltransferase provides a structural mechanism for activation by apolipoprotein A-I.
Q67833951A ‘Fish-eye disease’ familial condition with massive corneal opacities and hypoalphalipoproteinaemia: clinical, biochemical and genetic features
Q35797202Analysis of familial hypoalphalipoproteinemia syndromes
Q68486438Erythrocyte abnormalities in a hypoalphalipoproteinemia syndrome resembling fish eye disease
Q73359069Fish-eye disease: structural and in vivo metabolic abnormalities of high-density lipoproteins
Q34120460Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease
Q24564900Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met)

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