Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, CzVolume:
93
Language:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2013.09.012
Date:
November, 2013
File:
PDF, 2.09 MB
english, 2013