Matches in Nanopublications for { ?s ?p "[Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion description "[Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_provenance.
- assertion description "[Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion description "[Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.