Background: Mutations in a novel GTPase gene SPG3A cause an autosomal dominant hereditary spastic paraplegia linked to chromosome 14q (SPG3), which accounts f or approximately 10%to 15%of all autosomal dominant heredi...
supported by the National Key Basic Research Special Foundation(Nos.2010CB327605 and 2010CB328300);the National Natural Science Foundation of China(No.61307109);the National High Technology Research and Development Program of China(Nos.2013AA031501 and 2013AA013303);the Specialized Research Fund for the Doctoral Program of Higher Education(No.20120005120021);the Fundamental Research Funds for the Central Universities(No.2013RC1202)
A new receiver is proposed, which uses the fiber optical parametric amplifier(FOPA) in optical code division multiple access(OCDMA) over free space optic(FSO) communication system. The noise tolerance as the performan...