Novel Mutations in Serbian MEN1 Patients: Genotype-Phenotype Correlation
نویسندگان
چکیده
منابع مشابه
Novel mutations in FZD4 and phenotype–genotype correlation in Chinese patients with familial exudative vitreoretinopathy
PURPOSE To identify novel mutations in the frizzled 4 (FZD4) gene in patients with familial exudative vitreoretinopathy (FEVR) in southern China and to delineate the mutation-associated clinical manifestations. METHODS Clinical data and genomic DNA were collected from 100 probands and their family members. The coding regions of FZD4 were screened for mutations with PCR and Sanger sequencing. ...
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ژورنال
عنوان ژورنال: Journal of Medical Biochemistry
سال: 2018
ISSN: 1452-8266
DOI: 10.1515/jomb-2018-0013