Matches in Nanopublications for { ?s ?p "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879458.RAqK49aS9QLF2LS7YH0jmL_-lmt_NzSlfptpq9OE7P9Uw130_provenance.
- NP368961.RA8guZ4zjJ9MtGqjzuqSBDtOYLgSOCHzC8AA9wocwFOw4130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368961.RA8guZ4zjJ9MtGqjzuqSBDtOYLgSOCHzC8AA9wocwFOw4130_provenance.
- NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- NP180113.RAmyaelHe1MoIQ_3WLul1-Bhti3Whgmt-tr1pI7G9lu_Q130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180113.RAmyaelHe1MoIQ_3WLul1-Bhti3Whgmt-tr1pI7G9lu_Q130_provenance.
- NP368797.RAa573OrIC9NHdG3-KlICGmeV_giM6Ob5CISdZaeYEY5I130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368797.RAa573OrIC9NHdG3-KlICGmeV_giM6Ob5CISdZaeYEY5I130_provenance.
- NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- NP351202.RASHgmUXmIhiAtAZ-Pek0RmyT6FewsDyDPe5CpAdfNIYs130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351202.RASHgmUXmIhiAtAZ-Pek0RmyT6FewsDyDPe5CpAdfNIYs130_provenance.
- assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP563316.RAB1abZoFjmJLbrBOiGfQfwYaJ_SGnTR87Qjg93VZ-M6E130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563316.RAB1abZoFjmJLbrBOiGfQfwYaJ_SGnTR87Qjg93VZ-M6E130_provenance.
- NP846658.RAONl0hopgctTQEln7_-nHZMqkeQfCeK6CoYOX0atAaCc130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846658.RAONl0hopgctTQEln7_-nHZMqkeQfCeK6CoYOX0atAaCc130_provenance.
- NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- NP316028.RA1Km7_zLSf05qo4hXXuqIrSHXlNk0--vrZRku2XP0Q6A130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316028.RA1Km7_zLSf05qo4hXXuqIrSHXlNk0--vrZRku2XP0Q6A130_provenance.
- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.