Mutation spectrum of phenylketonuria in Syrian population: Genotype–phenotype correlation
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference41 articles.
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2. Mutation analysis of the phenylalanine hydroxylase gene of phenylketonuria patients of Kemerovskaya Oblast and Saha Republic;Baturina;Tsitol. Genet.,2012
3. Genotype–phenotype correlations analysis of mutations in the phenylalanine hydroxylase (PAH) gene;Bercovich;J. Hum. Genet.,2008
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5. Functional and structural characterization of novel mutations and genotype–phenotype correlation in 51 phenylalanine hydroxylase deficient families from Southern Italy;Daniele;FEBS J.,2009
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3. Mapping the Diverse Genetic Disorders and Rare Diseases Among the Syrian Population: Implications on Refugee Health and Health Services in Host Countries;Journal of Immigrant and Minority Health;2020-03-14
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