Pages that link to "Q35125990"

The following pages link to DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy (Q35125990):

Displaying 15 items.

• Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy (Q28084979) (← links)
• A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3 (Q29614852) (← links)
• Clinical outcome measures for trials in Duchenne muscular dystrophy: report from International Working Group meetings (Q30514152) (← links)
• Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing (Q33843901) (← links)
• Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice (Q34194689) (← links)
• Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene (Q34221402) (← links)
• Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort (Q36116293) (← links)
• Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells. (Q36278519) (← links)
• The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States (Q37607062) (← links)
• Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients? (Q38014906) (← links)
• Correlation of knee strength to functional outcomes in Becker muscular dystrophy (Q45752246) (← links)
• Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community. (Q52598175) (← links)
• Clinical Utility Gene Card for: Becker muscular dystrophy. (Q54269189) (← links)
• Single amino acid loss in the dystrophin protein associated with a mild clinical phenotype. (Q55008986) (← links)
• Becker muscular dystrophy caused by exon 2-truncating mutation of DMD (Q91387543) (← links)