Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegia.
Autorzy:
Qiu Y; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.; Rare Disease Center, The First Affiliated Hospital of Nanchang University, Nanchang, China. Xiong Y; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China. Wang L; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China. Zhu M; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.; Rare Disease Center, The First Affiliated Hospital of Nanchang University, Nanchang, China. TanD; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.; Rare Disease Center, The First Affiliated Hospital of Nanchang University, Nanchang, China. Hong D; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.; Rare Disease Center, The First Affiliated Hospital of Nanchang University, Nanchang, China.; Institute of Neurology, Jiangxi Academy of Clinical Medical Science, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China.; Key Laboratory of Rare Neurological Diseases of Jiangxi Provincial Health Commission, Jiangxi Medical College, Nanchang University, Nanchang, China.
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