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Annals of Hematology

Volumn 89, Issue 8, 2010, Pages 835-836

Protein C (PROC) gene mutations in two Indian families with purpura fulminans

(3) Pai, Navin a Shetty, Shrimati a Ghosh, Kanjaksha a

a KEM HOSPITAL (India)

Author keywords

[No Author keywords available]

Indexed keywords

CEFOTAXIME; CEFTRIAXONE; ENOXAPARIN; FRESH FROZEN PLASMA; HEPARIN; LINEZOLID; PROTEIN C; VITAMIN K GROUP; WARFARIN;

ANTICOAGULANT THERAPY; BLADDER OBSTRUCTION; BLOOD TRANSFUSION; BRAIN ISCHEMIA; BRAIN RADIOGRAPHY; CASE REPORT; CHILD DEATH; CLINICAL EVALUATION; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONSANGUINEOUS MARRIAGE; DISEASE MARKER; DISEASE SEVERITY; ECHOOCULOGRAPHY; FULMINATING PURPURA; GENE DELETION; GENETIC CONSERVATION; GENETIC PREDISPOSITION; HEMATOMA; HETEROZYGOTE; HUMAN; HYDRONEPHROSIS; HYDROURETER; INDIAN; JOINT NECROSIS; LETTER; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NEWBORN; PRIORITY JOURNAL; PROTEIN C DEFICIENCY; SAGITTAL SINUS THROMBOSIS; SCROTUM DISORDER; SKIN DISCOLORATION; THROMBOPHILIA; VITREOUS HEMORRHAGE; WOUND HEALING; FATALITY; FEMALE; GENETICS; INDIA; MALE; MUTATION; NUCLEOTIDE SEQUENCE;

DNA MUTATIONAL ANALYSIS; FATAL OUTCOME; FEMALE; HUMANS; INDIA; INFANT, NEWBORN; MALE; MUTATION; PROTEIN C; PROTEIN C DEFICIENCY; PURPURA FULMINANS;

EID: 77954668044 PISSN: 09395555 EISSN: None Source Type: Journal
DOI: 10.1007/s00277-009-0893-5 Document Type: Letter

Times cited : (4)

References (5)

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2
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- Homozygous protein C deficiency manifestated by massive venous thrombosis in the newborn
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3
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- Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: Evidence for solvent-induced bends in DNA heteroduplexes
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- Ganguly, A.¹ Rock, M.J.² Prockop, D.J.³

4
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- Compound heterozygous protein C deficiency caused by two mutations, Arg- 178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein C
- Sugahara Y, Miura O, Hirosawa S, Aoki N (1994) Compound heterozygous protein C deficiency caused by two mutations, Arg- 178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein C. Thromb Haemost 72:814-818
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5
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- Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.