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- NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_assertion type Assertion NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_head.
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- NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_assertion wasDerivedFrom gad-20150221 NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_provenance.
- NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_assertion SIO_000772 17594340 NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_provenance.
- NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_assertion evidence source_evidence_literature NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_provenance.
- NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_assertion description "[Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108617.RAALfcTZk9TdZie1iSUbor9MmPhzaW0ItE05AFdTE_A0o130_provenance.