,SCLT1

Monika K Grudzinska Pechhacker1,2, Anna Molnar1,2, Nadja Pekkola Pacheco3,4

  • 1Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

Ophthalmic genetics
|May 29, 2023
PubMed
概括

这项研究确定了一家家庭中SCLT1相关的轻度纤毛病症,其特点是形光感受器功能障碍和ADHD. 对于无法解释的视觉和神经发育障碍,进一步诊断至关重要.

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