Ebermann, Inga;
Scholl, Hendrik P. N.;
Charbel Issa, Peter;
Becirovic, Elvir;
Lamprecht, Jürgen;
Jurklies, Bernhard;
Millán, José M.;
Aller, Elena;
Mitter, Diana;
Bolz, Hanno
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
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Media type:
E-Article
Title:
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
Contributor:
Ebermann, Inga;
Scholl, Hendrik P. N.;
Charbel Issa, Peter;
Becirovic, Elvir;
Lamprecht, Jürgen;
Jurklies, Bernhard;
Millán, José M.;
Aller, Elena;
Mitter, Diana;
Bolz, Hanno
imprint:
Springer Science and Business Media LLC, 2007