Gaucher disease associated with a unique Kphl restriction site: identification of the amino-acid substitution
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1990.tb00371.x/fullpdf
Reference14 articles.
1. A comprehensive set of sequence analysis programs for the VAX
2. The human glucocerebrosidase gene and pseudogene: Structure and evolution
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