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ArticleGenetics and molecular biology

A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene.

Fábio Tadeu Arrojo Martins et al.PubMed ↗Full text ↗Publisher ↗

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3 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 30534854