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publicationName Orphanet Journal of Rare Diseases
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bibliographicCitation Yang D, Cho S, Cho SI, Kim M, Seong M, Park SS. Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene. Orphanet Journal of Rare Diseases. 2022 Mar 04;17(1):111. doi: 10.1186/s13023-022-02251-7.
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date 2022-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/35246191
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https://pubmed.ncbi.nlm.nih.gov/
title Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene
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Total number of triples: 37.