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Article

DNA microarray analysis for the detection of mutations in hemophilia A.

Journal of thrombosis and haemostasis : JTH - 1 Aug 2006

Berber E, Leggo J, Brown C, Berber E, Gallo N, Feilotter H, Lillicrap D

Abstract excerpt

BACKGROUND: Congenital deficiency of factor (F) VIII results in the inherited X-linked bleeding disorder hemophilia A. More than 900 different mutations are reported in the hemophilia A mutation database with the largest number of mutations being single nucleotide substitutions distributed throughout the gene. Complicating the molecular characterization of this disease is the complexity of the F8 gene, the...

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PMID: 16879218
DOI: 10.1111/j.1538-7836.2006.02055.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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