“We reanalyzed the patient’s genetic and clinical data and that brought us to a gene, FLVCR1, and a medical mystery to solve,” Calame said. One gene, multiple conditions To try to understand ...

Researchers identified rare genetic mutations that may account for undiagnosed neurodevelopmental disorders, linking the FLVCR1 gene with various neurological symptoms. A collaborative study, led by ...

However, it turns out that they all had conditions caused by a mutation in the same gene, called FLVCR1, according to new research set to be published in the journal Genetics in Medicine.

11月12日消息，贝勒医学院、新加坡国立大学等多家机构的研究人员对30名患有未知疾病的患者进行了基因检测，揭示了 FLVCR1 基因在罕见疾病发展中的作用。他们的研究发表在《医学遗传学 ...

"We reanalyzed the patient's genetic and clinical data and that brought us to a gene, FLVCR1, and a medical mystery to solve, ...