Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect

Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene

Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy

The heteroplasmic m.14709T>C mutation in the tRNAGlu gene in two Tunisian families with mitochondrial diabetes

A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene

International audience Background: Co-occurrence of two genetic diseases is challengi

Evidence for linkage and association between autoimmune thyroid diseases and the 18q12–q21 region in a large Tunisian family

Summary Many studies have shown linkage between IDDM6 locus on 18q12–q21 chromosome and several aut

<scp>l</scp>‐2‐Hydroxyglutaric aciduria: Clinical and molecular study in three Tunisian families. Identification of a new mutation and inter‐familial phenotype variability

Summary We report clinical and molecular studies in three unrelated Tunisian families containing se