Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome Sequencing

Bathing suit ichthyosis caused by a <i>TGM1</i> mutation in a Tunisian child

Abstract Background

Whole-exome sequencing of Ethiopian patients with ichthyosis vulgaris and atopic dermatitis

Carrier Frequency of the c.525delT Mutation in the <i>SGCG</i> Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population

Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan

Next-generation sequencing is commonly used to screen for pathogenic mutations in families with Mend

Duchenne muscular dystrophy in Niger: a family history

Duchenne muscular dystrophy is an inherited disease characterized by progressive muscle degeneration

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness