Associated Papers
The mutation spectrum and ethnic distribution of non-hepatorenal tyrosinemia (types II, III).
Beyzaei Z et al.
Orphanet Journal of Rare Diseases, 2022
Genetics and genomic medicine in Tunisia.
Elloumi-Zghal H et al.
Molecular Genetics & Genomic Medicine, 2018
Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.
Bouyacoub Y et al.
Gene, 2013
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