Published research expands clinical understanding of Pseudo-TORCH syndrome type 2 through discovery of an unreported variant ...

Indian scientists from Indira Gandhi Institute of Child Health, have uncovered a rare USP18 gene mutation causing repeated ...

Redcliffe Labs reports a groundbreaking discovery of a novel USP18 gene mutation associated with a rare neurological disorder ...

Bengaluru: Paediatricians in the city have documented what is said to be India's first known case of an ultra-rare genetic disorder — Pseudo-TORCH syn.

Indian researchers identify a novel USP18 gene mutation linked to pseudo-TORCH syndrome, aiding treatment for affected ...

Indian researchers have reported a rare USP18 gene mutation linked to repeated neurological decline in children. The mutation ...

A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children.

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 ...

Indian researchers have identified a novel gene mutation causing pseudo-TORCH Syndrome Type 2 in a child from a consanguineous marriage, using exome sequencing.

Doctors confirm rare gene mutation in child which causes changes in how immune system behaves during early development ...

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 ...