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Jianfan Chen Selected Research

Type III Amelogenesis Imperfecta

5/2021The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family.

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Jianfan Chen Research Topics

Disease

1Type III Amelogenesis Imperfecta
05/2021
1Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
05/2021
1Neoplasms (Cancer)
12/2017
1Prostatic Neoplasms (Prostate Cancer)
12/2017
1beta-Thalassemia (Cooley's Anemia)
10/2017

Drug/Important Bio-Agent (IBA)

1Proteins (Proteins, Gene)FDA Link
05/2021
1DystrophinIBA
05/2021
1Nonsense Codon (Nonsense Mutation)IBA
05/2021
1Therapeutic UsesIBA
12/2017
1TriterpenesIBA
12/2017
1GlobinsIBA
10/2017
1DNA (Deoxyribonucleic Acid)IBA
10/2017