ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.
Rohacek, Alex M
ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development. [electronic resource] - Developmental cell 11 2017 - 318-331.e5 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
1878-1551
10.1016/j.devcel.2017.09.026 doi
Alternative Splicing--genetics
Animals
Cell Differentiation--genetics
Cochlea--embryology
Hearing Loss--genetics
Mice, Knockout
Mutation--genetics
RNA-Binding Proteins--genetics
ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development. [electronic resource] - Developmental cell 11 2017 - 318-331.e5 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
1878-1551
10.1016/j.devcel.2017.09.026 doi
Alternative Splicing--genetics
Animals
Cell Differentiation--genetics
Cochlea--embryology
Hearing Loss--genetics
Mice, Knockout
Mutation--genetics
RNA-Binding Proteins--genetics