Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP421688.RA4WxGNzy7_m86mC2VHGZ92GdbKGmfHqf2dWyE6DxXGMM130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421688.RA4WxGNzy7_m86mC2VHGZ92GdbKGmfHqf2dWyE6DxXGMM130_provenance.
- NP191553.RA6oGaeEpGUv7RT538S7hWnJMstFVmWU9T5PcInxw4ENE130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191553.RA6oGaeEpGUv7RT538S7hWnJMstFVmWU9T5PcInxw4ENE130_provenance.
- NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- NP670593.RAyfPAExD5Mq3hcvMsDM57HvPFl--4DRjicHg9rBAfWPE130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670593.RAyfPAExD5Mq3hcvMsDM57HvPFl--4DRjicHg9rBAfWPE130_provenance.
- assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP834002.RAmgGxcIC5RK6VarzZN_MaxGaySBgKHDPR1BLCkxJ4RmE130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834002.RAmgGxcIC5RK6VarzZN_MaxGaySBgKHDPR1BLCkxJ4RmE130_provenance.
- NP856468.RAxKWi_kvp3DYYBX2jz8E1-gecOQsX7ujf5CtPpMijI00130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856468.RAxKWi_kvp3DYYBX2jz8E1-gecOQsX7ujf5CtPpMijI00130_provenance.