Matches in Nanopublications for { ?s ?p "[Overall, our data confirm that SPG7 point mutations are rare causes of HSP, in both sporadic and familial forms, while underlying the puzzling and intriguing aspects of histological and biochemical consequences of paraplegin loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP450498.RAPNQaNFI-aQJW-x6H1TW4vDLCHzWOYRXv_fDYTMN_G84130_assertion description "[Overall, our data confirm that SPG7 point mutations are rare causes of HSP, in both sporadic and familial forms, while underlying the puzzling and intriguing aspects of histological and biochemical consequences of paraplegin loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450498.RAPNQaNFI-aQJW-x6H1TW4vDLCHzWOYRXv_fDYTMN_G84130_provenance.
- assertion description "[Overall, our data confirm that SPG7 point mutations are rare causes of HSP, in both sporadic and familial forms, while underlying the puzzling and intriguing aspects of histological and biochemical consequences of paraplegin loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.