Article
Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.
Thrombosis and haemostasis - 1 Nov 2005
Johansson Anna M, Hillarp Andreas, Säll Torbjörn, Zöller Bengt, Dahlbäck Björn, Halldén Christer
Abstract excerpt
UNLABELLED: Protein S deficiency is an autosomal dominant disorder that results from mutations in the PROS1 gene. Conventional mutation detection techniques fail to detect a pathogenic PROS1 mutation in approximately 50% of cases. The present study investigates whether large deletions of PROS1 are found in families where mutations in the PROS1 gene have not been found despite sequencing. For this purpose,a dense...
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