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Article

Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families

28 Oct 2018

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30394349
DOI: 10.1016/j.ejmg.2018.10.013

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Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian familiesPMID 30394349Read ↗

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