1 results match your criteria: "Royal College of Surgeons in Ireland-Medical University of Bahrain Busaiteen Kingdom of Bahrain.[Affiliation]"
Galactosialidosis (GS, OMIM #256540) is a systemic autosomal recessive disorder that is due to a mutation in the cathepsin A (CTSA) gene. Its worldwide prevalence is rare, accounting for ~146 cases reported cases globally. In Bahrain alone, nine cases have been confirmed.
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