Redcliffe Labs diagnoses India’s first case of DPH2-Related Diphthamide Deficiency Syndrome-2 Identifying the DPH2 gene mutation enables healthcare providers to consider genetic counselling for families with a history of…
Redcliffe Labs study unveils rare genetic findings to help diagnose SENEBAC Syndrome in children The research has uncovered a rare NRROS gene mutation linked to SENEBAC syndrome, improving understanding of this severe…
