DNABCL11B

Ivana Lessel1, Anja Baresic2, Ivan K Chinn3

  • 1Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany; Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany.

PubMed
概括

关键发育基因BCL11B的遗传变异会导致明显的神经发育障碍. BCL11B变异的严重程度和类型与特定的临床亚型相关,并影响DNA结合,影响疾病结果.

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