A case report of hereditary sensory and autonomic neuropathy with retinopathy caused by FLVCR1 gene mutation
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A case report of hereditary sensory and autonomic neuropathy with retinopathy caused by FLVCR1 gene mutation
Journal of Chongqing Medical UniversityVol. 47, Issue 3, Pages: 351-354(2022)
作者机构:
1. 河南中医药大学儿科医学院,郑州,450000
2. 河南中医药大学第一附属医院儿科,郑州,450000
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Published:2022,
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Peng Yanyan, Feng Bin, Jiang Xianhe, et al. A case report of hereditary sensory and autonomic neuropathy with retinopathy caused by FLVCR1 gene mutation. [J]. Journal of Chongqing Medical University 47(3):351-354(2022)
DOI:
Peng Yanyan, Feng Bin, Jiang Xianhe, et al. A case report of hereditary sensory and autonomic neuropathy with retinopathy caused by FLVCR1 gene mutation. [J]. Journal of Chongqing Medical University 47(3):351-354(2022)DOI:
A case report of hereditary sensory and autonomic neuropathy with retinopathy caused by FLVCR1 gene mutation