P2RX2 exon-2 indel disrupts splicing and reduces receptor output in one DFNA41 family
A single-family functional study found that a heterozygous P2RX2 exon-2 insertion-deletion caused aberrant splicing and reduced P2X2 output, supporting a ...
A single-family functional study found that a heterozygous P2RX2 exon-2 insertion-deletion caused aberrant splicing and reduced P2X2 output, supporting a ...
© 2025 Scienmag - Science Magazine
© 2025 Scienmag - Science Magazine