22q11.2 deletion syndrome (22q) raises schizophrenia threat by means of cranium malformations linked to the Tbx1 gene, affecting cerebellar improvement. This highlights how non-brain components like bone defects can affect neurological problems. The chromosomal dysfunction 22q11.2 deletion syndrome (22q) has emerged as one of many strongest threat components for schizophrenia. Scientists at St. Jude Kids’s Analysis Hospital […]
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