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