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Intrafamilial Variability of the Deafness and Goiter Phenotype in Pendred Syndrome Caused by a T416P Mutation in the SLC26A4 Gene
Napiontek, Ulrike, Borck, Guntram, Müller-Forell, Wiebke, Pfarr, Nicole, Bohnert, Andrea, Keilmann, Annerose, Pohlenz, JoachimVolume:
89
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jc.2004-1013
Date:
November, 2004
File:
PDF, 250 KB
english, 2004