Matches in Nanopublications for { ?s ?p "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- NP678461.RAvjHQHIUeXV1TPKOON99Ey9t3c4KmXLOsusQ_JXNoKJM130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678461.RAvjHQHIUeXV1TPKOON99Ey9t3c4KmXLOsusQ_JXNoKJM130_provenance.
- NP830815.RA-HMlOkPfE4cuBeKnn04nYVwrk-hRal02EDZvvC6T04E130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830815.RA-HMlOkPfE4cuBeKnn04nYVwrk-hRal02EDZvvC6T04E130_provenance.
- NP871449.RAesR1NoAKejQBLox40t9wLtTSRU4LTx9c2yY2v20k5yc130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871449.RAesR1NoAKejQBLox40t9wLtTSRU4LTx9c2yY2v20k5yc130_provenance.
- NP871466.RAYiBDbP_Ups9_K4i1Gecoid1urDhJNVtJrM8chrKc3Eo130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871466.RAYiBDbP_Ups9_K4i1Gecoid1urDhJNVtJrM8chrKc3Eo130_provenance.
- assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP871432.RApFzXcjCtB2qkJx2YqpY-fCi4Z6pBzwIpl5Y57lwjYFU130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871432.RApFzXcjCtB2qkJx2YqpY-fCi4Z6pBzwIpl5Y57lwjYFU130_provenance.
- NP969846.RANEYT5bzJAWSGoluscImE5bVSVYg0R1cuNv7iOAFKGz8130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969846.RANEYT5bzJAWSGoluscImE5bVSVYg0R1cuNv7iOAFKGz8130_provenance.
- NP969848.RA8scHCWginP3TYYf4LOFn4BJ6ixtoGQ2nosIFULwNWyU130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969848.RA8scHCWginP3TYYf4LOFn4BJ6ixtoGQ2nosIFULwNWyU130_provenance.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_provenance.