(PDF) GT to AT Transition at a Splice Donor Site Causes

GT to AT Transition at a Splice Donor Site Causes Skipping of the Preceding Exon in Phenylketonuria

Nucleic Acids Research - United Kingdom

doi 10.1093/nar/15.14.5613

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January 1, 1987

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Oxford University Press (OUP)

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GT to AT Transition at a Splice Donor Site Causes Skipping of the Preceding Exon in Phenylketonuria

Nucleic Acids Research - United Kingdom

doi 10.1093/nar/15.14.5613

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

A T+6 to C+6 Mutation in the Donor Splice Site of COL3A1 IVS7 Causes Exon Skipping and Results in Ehlers-Danlos Syndrome Type IV.

Ab Initio Prediction of Mutation-Induced Cryptic Splice-Site Activation and Exon Skipping

Identification of a Novel Exonic Mutation at -13 From 5' Splice Site Causing Exon Skipping in a Girl With Mitochondrial Acetoacetyl-Coenzyme a Thiolase Deficiency.

A Mutation Hotspot at the P14ARF Splice Site

A Novel Splice-Site Mutation on the MLC1 Gene Leading to Exon 9 Skipping and Megalencephalic Leukoencephalopathy With Subcortical Cysts in a Turkish Patient

Autoregulation of the Human Splice Factor Kinase CLK1 Through Exon Skipping and Intron Retention

A Novel Type 2A Von Willebrand Factor Mutation Located at the Last Nucleotide of Exon 26 (3538G>A) Causes Skipping of 2 Nonadjacent Exons

Exon, Intron and Splice Site Locations in the Spliceosomal B Complex

Exon-Skipping Splice Variants of Excitatory Amino Acid Transporter-2 (EAAT2) Form Heteromeric Complexes With Full-Length EAAT2