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A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers crucial insights into a neurological ...
Indian scientists from Indira Gandhi Institute of Child Health, have uncovered a rare USP18 gene mutation causing repeated brain problems in kids, bringing India's first case of this ultra-rare ...
New Delhi: Redcliffe Labs has identified a previously unknown USP18 gene mutation associated with a rare pediatric neurological disorder, marking the first such discovery in India and contributing new ...
New Delhi, Nov 27: 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 ...
A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers crucial insights into a neurological ...
New Delhi, November 27 (IANS): A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers crucial ...