Protein C London 1: recurrent mutation at Arg 169 ...[Nucleic Acids Res. 1989] - PubMed Result

SearchDatabase nameforSearch term

Advanced Search

Your browser version may not work well with NCBI's Web applications. More information here...

Display Show

All: 1

Review: 0

Click to change filter selection through MyNCBI.

1: Nucleic Acids Res. 1989 Dec 25;17(24):10513. Links

Protein C London 1: recurrent mutation at Arg 169 (CGG----TGG) in the protein C gene causing thrombosis.

Grundy C, Chitolie A, Talbot S, Bevan D, Kakkar V, Cooper DN.

Molecular Genetics Section, King's College Hospital Medical School, Denmark Hill, London, UK.

PMID: 2602169 [PubMed - indexed for MEDLINE]

PMCID: PMC335338

Related articles

A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis.
Blood Coagul Fibrinolysis. 1993 Apr; 4(2):345-7.

[Blood Coagul Fibrinolysis. 1993]
Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosis.
Hum Genet. 1992 Aug; 89(6):685-6.

[Hum Genet. 1992]
An abnormal protein C (protein C Yonago) with an amino acid substitution of Gly for Arg-15 caused by a single base mutation of C to G in codon 57 (CGG-->GGG). Deteriorated calcium-dependent conformation of the gamma-carboxyglutamic acid domain relevant to a thrombotic tendency.
Int J Hematol. 1993 Jan; 57(1):9-14.

[Int J Hematol. 1993]
Review[Point mutation G-->A nucleotide 1691 factor V gene as a cause of developing thrombotic complications in a family with plasma resistance to activated protein C]
Pol Arch Med Wewn. 1996 May; 95(5):464-70.

[Pol Arch Med Wewn. 1996]
ReviewActivated protein C resistance--a major risk factor for thrombosis.
Eur J Clin Chem Clin Biochem. 1997 Jul; 35(7):501-16.

[Eur J Clin Chem Clin Biochem. 1997]
» See reviews... | » See all...

Cited by 1 PubMed Central article

Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.
Yamamoto K, Tanimoto M, Emi N, Matsushita T, Takamatsu J, Saito H. J Clin Invest. 1992 Dec; 90(6):2439-46.

[J Clin Invest. 1992]

Recent Activity

Clear Turn Off Turn On

Protein C London 1: recurrent mutation at Arg 169 (CGG----TGG) in the protein C gene causi...Protein C London 1: recurrent mutation at Arg 169 (CGG----TGG) in the protein C gene causing thrombosis.

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Display Show