在一个独特的家族中识别发育性色彩不可知症的候选基因

Tanja C W Nijboer1,2, Ellen V S Hessel1,3, Gijs W van Haaften3

  • 1UMCU Brain Center and Center of Excellence for Rehabilitation Medicine, University Medical Center Utrecht and De Hoogstraat Rehabilitation, Utrecht, The Netherlands.

PloS one
|September 6, 2023
PubMed
概括

研究人员确定了与神经功能相关的基因中的罕见遗传变异,这些变异发生在一个患有遗传发育色彩无知症的家族中. 这项研究为了解这种罕见的大脑疾病提供了起点.

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