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Updated: Jan 31, 2026

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
Published on: January 3, 2015
A novel frameshift deletion in NAGLU causing sanfilipo type III-B in an Indian family
Sweta Jain1, Vamsee Chaitanya2, Mohammed Faruq1
1Genomics and Molecular Medicine CSIR-Institute of Genomics and Integrative Biology New Delhi India.
Abstract:
Mucopolysaccharidoses are group of inherited lysosomal storage disorder. Two siblings of a family manifested behavioral abnormalities; hepatosplenomegaly and hypotonia of infantile onset were found to have a novel homozygous frameshift variation, p.Leu280TrpfsTer19 in NAGLU. This variant was predicted to cause the loss of TIM-barrel and alpha-helical region of NAGLU protein.
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