SCOPUS 정보 검색 플랫폼

Annals of Hematology

Volumn 91, Issue 10, 2012, Pages 1667-1668

Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation

(4) Kulkarni, B a Kanakia, S b Ghosh, K a Shetty, S a

a KEM HOSPITAL (India)

b LILAVATI HOSPITAL AND RESEARCH CENTRE (India)

Author keywords

[No Author keywords available]

Indexed keywords

FIBRINOGEN; FRESH FROZEN PLASMA; VITAMIN K GROUP;

AMINO ACID SUBSTITUTION; BLOOD SAMPLING; BRAIN HEMORRHAGE; CASE REPORT; CLINICAL FEATURE; DISEASE SEVERITY; DNA FLANKING REGION; DNA SEQUENCE; FEMALE; GENETIC ASSOCIATION; HUMAN; INFANT; LETTER; MEDICAL HISTORY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PARTIAL THROMBOPLASTIN TIME; POLYMERASE CHAIN REACTION; PREDICTION; PRIORITY JOURNAL; PROTHROMBIN DEFICIENCY; PROTHROMBIN TIME; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS; SUBDURAL HEMATOMA; THROMBIN TIME; TREATMENT RESPONSE;

CYSTEINE; FEMALE; HUMANS; HYPOPROTHROMBINEMIAS; INFANT; MUTATION; PROTHROMBIN; SERINE; SEVERITY OF ILLNESS INDEX;

EID: 84867337550 PISSN: 09395555 EISSN: 14320584 Source Type: Journal
DOI: 10.1007/s00277-012-1442-1 Document Type: Letter

Times cited : (3)

References (8)

1
- 0023175705
- Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively
- Royle NJ, Irwin DM, Koschinsky ML, MacGillivray RT, Hamerton JL (1987) Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively. Somat Cell Mol Genet 13:285-292
- (1987) Somat Cell Mol Genet , vol.13 , pp. 285-292
- Royle, N.J.¹ Irwin, D.M.² Koschinsky, M.L.³ MacGillivray, R.T.⁴ Hamerton, J.L.⁵

2
- 84872220874
- Accessed January 2011
- Human genome mutation database, f2 gene. http://www.hgmd.cf.ac.uk/ac/ gene.php?gene0FII. Accessed January 2011
- Human Genome Mutation Database, f2 Gene

3
- 0032525101
- Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
- De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M, Servidei S, Tonali PA, Leone G (1998) Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 91:3562-3565
- (1998) Blood , vol.91 , pp. 3562-3565
- De Stefano, V.¹ Chiusolo, P.² Paciaroni, K.³ Casorelli, I.⁴ Rossi, E.⁵ Molinari, M.⁶ Servidei, S.⁷ Tonali, P.A.⁸ Leone, G.⁹

4
- 67749084428
- Congenital prothrombin deficiency
- Lancellotti S, De Cristofaro R (2009) Congenital prothrombin deficiency. Semin Thromb Hemost 35:367-381
- (2009) Semin Thromb Hemost , vol.35 , pp. 367-381
- Lancellotti, S.¹ De Cristofaro, R.²

5
- 25144524061
- Molecular genetics of hereditary prothrombin deficiency in Indian patients: Identification of a novel Ala362- Thr (Prothrombin Vellore 1) mutation
- Jayandharan G,Viswabandya A, Baidya S, Nair SC, Shaji RV, Chandy M, Srivastava A (2005) Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362- Thr (Prothrombin Vellore 1) mutation. J Thromb Haemost 3:1446-1453
- (2005) J Thromb Haemost , vol.3 , pp. 1446-1453
- Jayandharan, G.¹ Viswabandya, A.² Baidya, S.³ Nair, S.C.⁴ Shaji, R.V.⁵ Chandy, M.⁶ Srivastava, A.⁷

6
- 84872214037
- Accessed January 2011
- NCBI gene, f2 gene. http://www.ncbi.nlm.nih.gov/sites/gene. Accessed January 2011
- NCBI Gene, f2 Gene

7
- 84872212489
- Accessed January 2011
- Clustral w2-multiple sequence alignment. http://www.ebi.ac.uk/Tools/ clustalw2/index.html. Accessed January 2011
- Clustral w2-multiple Sequence Alignment

8
- 84872213486
- Accessed January 2011
- Ensembl genome browser, f2 gene-human. http://www.ensembl.org/index.html. Accessed January 2011
- Ensembl Genome Browser, f2 Gene-human

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.