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- NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_assertion type Assertion NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_head.
- NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_provenance.
- NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_assertion evidence source_evidence_literature NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_provenance.
- NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_assertion SIO_000772 21139041 NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_provenance.
- NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_assertion wasDerivedFrom befree-20140225 NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_provenance.
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