Pages that link to "Q57562609"

The following pages link to The gene for a novel glycosyltransferase is mutated in congenital muscular dystrophy MDC1C and limb girdle muscular dystrophy 2I (Q57562609):

Displaying 11 items.

• The 10 autosomal recessive limb-girdle muscular dystrophies (Q35201105) (← links)
• The role of defective glycosylation in congenital muscular dystrophy (Q35824015) (← links)
• Diagnostic immunohistochemistry in neuromuscular disorders (Q36012956) (← links)
• ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies (Q36581125) (← links)
• Muscle protein alterations in LGMD2I patients with different mutations in the Fukutin-related protein gene (Q36942490) (← links)
• Intensity dependent confidence intervals on microarray measurements of differentially expressed genes: a case study of the effect of MK5, FKRP and TAF4 on the transcriptome. (Q42092635) (← links)
• Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagents (Q48259029) (← links)
• A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans (Q50911860) (← links)
• Chapter 31 Immunopathology and molecular genetics of dystrophinopathies (Q57562581) (← links)
• Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum (Q58052175) (← links)
• Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutation (Q79108265) (← links)