<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>260(9)</volume><submitter>Bettencourt C</submitter><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><funding>Parkinson's UK</funding><journal>Journal of neurology</journal><pagination>2414-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3764324</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment.</pubmed_title><pmcid>PMC3764324</pmcid><funding_grant_id>G1001253</funding_grant_id><funding_grant_id>G1100643</funding_grant_id><funding_grant_id>G0801418B</funding_grant_id><funding_grant_id>G-1107</funding_grant_id><funding_grant_id>G108/638</funding_grant_id><funding_grant_id>G0802760</funding_grant_id><funding_grant_id>MR/J004758/1</funding_grant_id><funding_grant_id>089698</funding_grant_id><funding_grant_id>MC_G1000735</funding_grant_id><funding_grant_id>G0700943</funding_grant_id><pubmed_authors>Houlden H</pubmed_authors><pubmed_authors>Bettencourt C</pubmed_authors><pubmed_authors>Singleton AB</pubmed_authors><pubmed_authors>Hardy J</pubmed_authors><pubmed_authors>Morris HR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment.</name><description/><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Sep</publication><modification>2025-04-04T07:54:00.092Z</modification><creation>2022-02-09T14:21:13.604Z</creation></dates><accession>S-EPMC3764324</accession><cross_references><pubmed>23881105</pubmed><doi>10.1007/s00415-013-7044-6</doi></cross_references></HashMap>