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The gene structure ofXenopusnuclear lamin A: A model for the evolution of A-type from B-type lamins by exon shuffling

✍ Scribed by Reimer Stick


Publisher
Springer
Year
1992
Tongue
English
Weight
994 KB
Volume
101
Category
Article
ISSN
0009-5915

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von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF). A large number of defects that cause qualitative variants have been located in the A1 domain of the vWF, which