Article Versions Notes

Zang L, Han Y, Zhang Q, Luo S, Hu Z, Xia K, Ahmed A, Tian Q. Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental Delay. International Journal of Molecular Sciences. 2025; 26(16):7820. https://doi.org/10.3390/ijms26167820

Zang, Liyu, Yaoling Han, Qiumeng Zhang, Si Luo, Zhengmao Hu, Kun Xia, Ashfaque Ahmed, and Qi Tian. 2025. "Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental Delay" International Journal of Molecular Sciences 26, no. 16: 7820. https://doi.org/10.3390/ijms26167820

Zang, L., Han, Y., Zhang, Q., Luo, S., Hu, Z., Xia, K., Ahmed, A., & Tian, Q. (2025). Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental Delay. International Journal of Molecular Sciences, 26(16), 7820. https://doi.org/10.3390/ijms26167820