Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease.

Wolf, Andreas

Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease. [electronic resource] - Human mutation Oct 2011 - 1137-43 p. digital

Publication Type: Journal Article

1098-1004

10.1002/humu.21547 doi


5' Flanking Region
Codon, Initiator
Consensus Sequence
Databases, Genetic
Genetic Diseases, Inborn--genetics
Humans
Mutation Rate
Open Reading Frames
Peptide Chain Initiation, Translational--genetics
Point Mutation