DNAJB6 myopathy: A vacuolar myopathy with childhood onset

DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions

(2013) Takatoshi Sato et al.   NEUROMUSCULAR DISORDERS

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy

(2012) Jaakko Sarparanta et al.   NATURE GENETICS

Update on the Genetics of Limb Girdle Muscular Dystrophy

(2012) Satomi Mitsuhashi et al.   Seminars in Pediatric Neurology

Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics

(2011) Steven A. Greenberg et al.   ANNALS OF NEUROLOGY

Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

(2011) Matthew B. Harms et al.   ANNALS OF NEUROLOGY

Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus

(2011) Peter Hackman et al.   NEUROMUSCULAR DISORDERS

The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophy

(2010) S. Sandell et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The HSP70 chaperone machinery: J proteins as drivers of functional specificity

(2010) Harm H. Kampinga et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia

(2009) Tanya Stojkovic et al.   NEUROMUSCULAR DISORDERS