Matches in Nanopublications for { ?s ?p "[We further suggest that loss of necdin contributes to the neurological phenotype of PWS, and raise the possibility that co-deletion of necdin and the related protein Magel2 may explain the lack of single gene mutations in PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion description "[We further suggest that loss of necdin contributes to the neurological phenotype of PWS, and raise the possibility that co-deletion of necdin and the related protein Magel2 may explain the lack of single gene mutations in PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_provenance.
- assertion description "[We further suggest that loss of necdin contributes to the neurological phenotype of PWS, and raise the possibility that co-deletion of necdin and the related protein Magel2 may explain the lack of single gene mutations in PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion description "[We further suggest that loss of necdin contributes to the neurological phenotype of PWS, and raise the possibility that co-deletion of necdin and the related protein Magel2 may explain the lack of single gene mutations in PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_provenance.