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The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung's disease https://t.co/YfG4mgnC0I
The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung's disease https://t.co/YfG4mgnC0I
New Research: The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease: Introduction: As a congenital and genetically related disease, many single nucleotide… #celldevbio https://t.co