由于SLC6A8的低形态变异引起的肌酸转运体缺乏症的治疗反应

Nicola Longo1, Laura Alane Voss2, Marta Frigeni3

  • 1Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, USA; Department of Pathology, University of Utah, USA; ARUP Laboratories, Salt Lake City, UT 84108, USA; Division of Clinical Genetics, Department of Human Genetics, University of California Los Angeles, Los Angeles, CA 90095, USA.

PubMed
概括

大脑肌酸缺乏综合征 (CCDS) 可能导致发育迟缓和语言问题. 这项研究表明,将肌酸载体活性降低到25%可以引起症状,补充可能有助于较轻微的病例.

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