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Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations

✍ Scribed by Sai Prasad; Karen A. Kölln; Robert A. Cucci; Richard C. Trembath; Guy Van Camp; Richard J.H. Smith


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
197 KB
Volume
124A
Category
Article
ISSN
1552-4825

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