Matches in Nanopublications for { ?s ?p "[It confirms PHOX2A as the autosomal recessive CFEOM2 disease gene and provides evidence that the phenotypic differences between PHOX2A mutations in man and mouse do not result from hypomorphic PHOX2A alleles in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[It confirms PHOX2A as the autosomal recessive CFEOM2 disease gene and provides evidence that the phenotypic differences between PHOX2A mutations in man and mouse do not result from hypomorphic PHOX2A alleles in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_assertion description "[It confirms PHOX2A as the autosomal recessive CFEOM2 disease gene and provides evidence that the phenotypic differences between PHOX2A mutations in man and mouse do not result from hypomorphic PHOX2A alleles in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.