Molecular basis of congenital lp (a) deficiency: a frequent apo (a)'null'mutation in caucasians

M Ogorelkova, A Gruber… - Human molecular …, 1999 - academic.oup.com
High plasma concentrations of lipoprotein (a)[Lp (a)], a covalent low-density lipoprotein-
apolipoprotein (a)[apo (a)] complex, are associated with coronary heart disease and stroke …
被引用次数：101 相关文章

Molecular basis of congenital lp (a) deficiency: a frequent apo (a)'null'mutation in caucasians

M Ogorelkova, A Gruber… - Human molecular …, 1999 - pubmed.ncbi.nlm.nih.gov
High plasma concentrations of lipoprotein (a)[Lp (a)], a covalent low-density lipoprotein-
apolipoprotein (a)[apo (a)] complex, are associated with coronary heart disease and stroke …

Molecular basis of congenital lp (a) deficiency: a frequent apo (a)'null'mutation in caucasians.

M Ogorelkova, A Gruber, G Utermann - Human Molecular Genetics, 1999 - europepmc.org
High plasma concentrations of lipoprotein (a)[Lp (a)], a covalent low-density lipoprotein-
apolipoprotein (a)[apo (a)] complex, are associated with coronary heart disease and stroke …

[引用][C] Molecular basis of congenital Lp (a) deficiency: a frequent apo (a)'null'mutation in Caucasians

M OGORELKOVA, A GRUBER… - Human molecular …, 1999 - pascal-francis.inist.fr
Molecular basis of congenital Lp(a) deficiency : a frequent apo(a) 'null' mutation in
Caucasians CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …

[引用][C] Molecular basis of congenital lp (a) deficiency: a frequent apo (a) null mutation in caucasians

M Ogorelkova, A Gruber, G Utermann - Human Molecular Genetics, 1999 - elibrary.ru
[PDF] researchgate.net

[PDF][PDF] Molecular basis of congenital Lp (a) deficiency: a frequent apo (a)'null'mutation in Caucasians

M Ogorelkova, A Gruber… - Human Molecular Genetics, 1999 - researchgate.net
High plasma concentrations of lipoprotein (a)[Lp (a)], a covalent low-density lipoprotein–
apolipoprotein (a)[apo (a)] complex, are associated with coronary heart disease and stroke …

Molecular basis of congenital Lp (a) deficiency: a frequent apo (a)'null'mutation in Caucasians.

M Ogorelkova, A Gruber… - Human Molecular …, 1999 - search.ebscohost.com
Examines a donor splice site mutation in the intron of apo (a) K IV type 8 intron which results
in a truncated form devoid of certain K IV types. Prevalence of the mutation among …

[引用][C] Molecular basis of congenital Lp (a) deficiency: a frequent apo (a)'null'mutation in Caucasians

M OGORELKOVA, A GRUBER… - Human molecular …, 1999 - Oxford University Press