Direct detection of factor IX gene deletions in Indian haemophiliacs by multiplex PCR [2]

European Journal of Haematology

Volumn 71, Issue 3, 2003, Pages 233-234

  Shetty, Shrimati ^a   Ghosh, Kanjaksha ^a   Mohanty, Dipika ^a  

^a KEM HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 9; PRIMER DNA;

DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DISEASE SEVERITY; DNA PROBE; EXON; GENE DELETION; HEMOPHILIA; HUMAN; INDIA; LETTER; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING; X CHROMOSOME LINKED DISORDER;

FACTOR IX; GENE DELETION; HEMOPHILIA B; HUMANS; INDIA; POLYMERASE CHAIN REACTION;

EID: 0042835374     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0609.2003.00119.x     Document Type: Letter

References (4)

1. GREEN PM, GIANELLI F, SOMMER SS, et al. The Haemophilia B mutation database - version 12. http://www.kcl.ac.uk/ip/petergreen/intro.html (accessed on 30-05-2003).
2. SHETTY S, GHOSH K, PATHARE A, COLAH R, BADAKERE S, MOHANTY D. Factor VIII and IX gene polymorphisms and carrier analysis in Indian population. Am J Haematol 1997;54:271-275.
3. SHETTY S, GHOSH K, PATHARE A, JIJINA F, MOHANTY D. Screening for mutations in haemophilia A and B patients by Southern Blotting technique. Haemophilia 1998;4:802-805.
4. COSTA JM, ERNAULT P, VIDAUD D, VIDAUD M, MEYER D, LAVERGNE JM. Fast and efficient mutation detection method using multiplex PCR and cycle sequencing. Thromb Haemost 2000;83:244-247.