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2. A splicing mutation in VPS4B causes dentin dysplasia I. Issue 9 (31st May 2016)

3. C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot–Marie–Tooth disease in a knockout mouse model. (27th June 2020)

8. Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation. (11th September 2021)