Indian scientists discover rare gene mutation behind repeated neurological disorders in children
NEW DELHI: Indian researchers have identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare ...
NEW DELHI: Indian researchers have identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare ...
New Delhi : The World Health Organization’s November 2024 report revealed that chronic obstructive pulmonary disease (COPD) remains the fourth ...
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