Associated Papers
Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders.
Bizzari S et al.
Genes, 2021
34680914 (PubMed )
Supplement: genes-12-01518-s001.zip › SupplementaryTableS2_26-09-2021.xlsx › CTGA-unique_variants
Experience with hyperphenylalaninemia in a developing country: unusual clinical manifestations and a novel gene mutation.
Karam PE et al.
Journal of Child Neurology, 2011
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