Indian scientists from Indira Gandhi Institute of Child Health, have uncovered a rare USP18 gene mutation causing repeated ...
In a major medical breakthrough, Indian researchers have identified a rare USP18 gene mutation linked to repeated neurological decline in children — the first such case ever reported from India. The ...
5don MSN
Indian scientists discover rare gene mutation behind repeated neurological disorders in children
Indian researchers have identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare ...
Greater Kashmir on MSN
Indian researchers find rare gene mutation linked to recurrent neurological decline in kids
A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children ...
In a major scientific breakthrough, Indian researchers have identified a novel mutation in the USP18 gene linked to recurrent neurological deterioration in children — marking the first such case ...
As Vande Mataram turns 150, DU students celebrate through cultural events. Dyal Singh marked its historic significance in VC's presence. LSR to celebrate soon.
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