reference/13868274

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endingPage	1332
issn	0002-9297
issueIdentifier	5
pageRange	1328-1332
publicationName	The American Journal of Human Genetics
startingPage	1328
bibliographicCitation	Hansen JJ, Dürr A, Cournu-Rebeix I, Georgopoulos C, Ang D, Nielsen MN, Davoine C, Brice A, Fontaine B, Gregersen N, Bross P. Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60. The American Journal of Human Genetics. 2002 May;70(5):1328–32. doi: 10.1086/339935.
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date	200205
identifier	https://pubmed.ncbi.nlm.nih.gov/11898127 https://doi.org/10.1086/339935 https://pubmed.ncbi.nlm.nih.gov/PMC447607
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
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Total number of triples: 71.