Comprehensive Molecular Diagnosis of 67 Chinese Usher Syndrome Probands: High Rate of Ethnicity Specific Mutations in Chinese USH Patients
Orphanet Journal of Rare Diseases - United Kingdom
doi 10.1186/s13023-015-0329-3
Full Text
Open PDFAbstract
Available in full text
Date
September 4, 2015
Authors
Publisher
Springer Science and Business Media LLC