Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

Published:2012-04 Issue:2 Volume:351 Page:342-350
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Cirello Valentina,Bazzini Claudia,Vezzoli Valeria,Muzza Marina,Rodighiero Simona,Castorina Pierangela,Maffini Antonia,Bottà Guido,Persani Luca,Beck-Peccoz Paolo,Meyer Giuliano,Fugazzola Laura

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference47 articles.

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3. Genetics and phenomics of Pendred syndrome;Bizhanova;Mol. Cell. Endocrinol.,2010

4. Distal renal tubular acidosis in mice that lack the forkhead transcription factor Foxi1;Blomqvist;J. Clin. Invest.,2004

5. Epididymal expression of the forkhead transcription factor Foxi1 is required for male fertility;Blomqvist;EMBO J.,2006

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