Open AccessIn-Frame Insertion Mutation in the SPG11 Gene Causes Autosomal Recessive Spastic Paraplegia with Thin Corpus Callosum âÂÂIn Aâ Turkish Family with Late Age of Onset of the Phenotype
Author(s) -
Moneef Shoukier,
Chiranjeevi Bodda
Publication year - 2015
Publication title -
journal of bioanalysis and biomedicine
Language(s) - English
Resource type - Journals
ISSN - 1948-593X
DOI - 10.4172/1948-593x.1000142
Subject(s) - hereditary spastic paraplegia , genetics , exon , gene , biology , mutation , missense mutation , mutant , stop codon , loss function , phenotype