Pages that link to "Q35238731"

The following pages link to Unusual patterns of exon skipping in Bruton tyrosine kinase are associated with mutations involving the intron 17 3' splice site. (Q35238731):

Displaying 7 items.

• Order of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-propeptides and Ehlers-Danlos syndrome type I (Q24612309) (← links)
• Two-exon skipping within MLPH is associated with coat color dilution in rabbits (Q27335075) (← links)
• Molecular and Structural Characterization of Five Novel Mutations in the Bruton’s Tyrosine Kinase Gene from Patients with X-Linked Agammaglobulinemia (Q30176486) (← links)
• A novel splice variant in the N-propeptide of COL5A1 causes an EDS phenotype with severe kyphoscoliosis and eye involvement (Q33911125) (← links)
• X-linked clonality testing: interpretation and limitations (Q34619256) (← links)
• Widespread intra-dependencies in the removal of introns from human transcripts (Q49208373) (← links)
• BTKbase, mutation database for X-linked agammaglobulinemia (XLA) (Q57269822) (← links)