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Anhui Qi

Peking Union Medical College

4

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A novel NHS mutation in a Chinese family with Nance‑Horan Syndrome

2019 Molecular Medicine Reports
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Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto’s thyroiditis

2018 BMC Endocrine Disorders
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A novel CRX frameshift mutation causing cone-rod dystrophy in a Chinese family: A case report

2018 Medicine
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Novel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease.

2016 Molecular Vision
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