Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility

Overview of attention for article published in Human Mutation, February 2020

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RT @cilia_biblios: Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy,…

RT @cilia_biblios: Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy,…

RT @elfridedebaere: Congrats to all who contributed! We also thank the patients.

Congrats to all who contributed! We also thank the patients.

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