<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>70(12)</volume><submitter>Benko WS</submitter><funding>Intramural NIH HHS</funding><journal>Neurology</journal><pagination>976-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4617237</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3.</pubmed_title><pmcid>PMC4617237</pmcid><funding_grant_id>Z99 HG999999</funding_grant_id><pubmed_authors>Goker-Alpan O</pubmed_authors><pubmed_authors>Benko WS</pubmed_authors><pubmed_authors>Hruska KS</pubmed_authors><pubmed_authors>Schiffmann R</pubmed_authors><pubmed_authors>Nagan N</pubmed_authors><pubmed_authors>Hart PS</pubmed_authors><pubmed_authors>Sidransky E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3.</name><description/><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Mar</publication><modification>2025-04-26T19:25:50.526Z</modification><creation>2025-04-06T16:06:49.854Z</creation></dates><accession>S-EPMC4617237</accession><cross_references><pubmed>18347322</pubmed><doi>10.1212/01.wnl.0000305963.37449.32</doi></cross_references></HashMap>