Lina Brodd
Publications by Year
Research Areas
Muscle Physiology and Disorders, Ubiquitin and proteasome pathways, RNA Research and Splicing, Protease and Inhibitor Mechanisms, Hypothalamic control of reproductive hormones
Most-Cited Works
- → Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan(2013)236 cited
- → Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan(2013)194 cited
- → ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies(2013)105 cited
- → Development of an L gene real-time reverse-transcription PCR assay for the detection of avian paramyxovirus type 1 RNA in clinical samples(2010)70 cited
- → G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies(2012)1 cited
- → Whole exome sequencing in congenital hypogonadotropic hypogonadism(2015)