UBAP1L--

Christina Zeitz1, Julien Navarro1, Leila Azizzadeh Pormehr2

  • 1Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

概括

在北非患者中,UBAP1L的新基因缺陷会导致遗传性视网膜退化 (IRD). 这一发现扩大了对IRD遗传学和视网膜失明的潜在治疗点的理解.

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