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Wiley, Human Mutation: Variation, Informatics and Disease, 11(41), p. 1871-1876, 2020

DOI: 10.1002/humu.24094

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Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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