Matches in Nanopublications for { ?s ?p "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 7 of
7
with 100 items per page.
- NP818269.RAfa23z9NEc7pIzrnSL5fGx5GGTpkPUdESxCLfy2Oo5y8130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818269.RAfa23z9NEc7pIzrnSL5fGx5GGTpkPUdESxCLfy2Oo5y8130_provenance.
- NP176623.RA4piXUW6W2hN4CByr0kFTyZxbgYh9SATEfpQS_odlmXE130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176623.RA4piXUW6W2hN4CByr0kFTyZxbgYh9SATEfpQS_odlmXE130_provenance.
- NP187950.RAROkh6GJ7t2SK0j8AvIx5LzLMFr9na_b6K7ZB1P2kVjs130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187950.RAROkh6GJ7t2SK0j8AvIx5LzLMFr9na_b6K7ZB1P2kVjs130_provenance.
- NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527774.RADccuyaPgyNz4WMiPa4OGihOuFe6AcIhAKgdSfriydz4130_provenance.
- NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- NP258679.RA5Medc1NpKW0J0YBLRKAx0AkN7Oyrl514rVuTCEqmbbU130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258679.RA5Medc1NpKW0J0YBLRKAx0AkN7Oyrl514rVuTCEqmbbU130_provenance.
- assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.