<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(6)</volume><submitter>Fan LL</submitter><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Hunan Province</funding><journal>Genes &amp; diseases</journal><pagination>1412-1414</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9485271</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy.</pubmed_title><pmcid>PMC9485271</pmcid><funding_grant_id>81470445</funding_grant_id><funding_grant_id>2020JJ5785</funding_grant_id><funding_grant_id>81970268</funding_grant_id><funding_grant_id>82000427</funding_grant_id><pubmed_authors>Jiao ZJ</pubmed_authors><pubmed_authors>Fan LL</pubmed_authors><pubmed_authors>Yang YF</pubmed_authors><pubmed_authors>Tan ZP</pubmed_authors><pubmed_authors>Zeng H</pubmed_authors><pubmed_authors>Yuan ZZ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy.</name><description/><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-07-14T15:49:30.319Z</modification><creation>2025-04-04T21:35:20.819Z</creation></dates><accession>S-EPMC9485271</accession><cross_references><pubmed>36157493</pubmed><doi>10.1016/j.gendis.2022.02.011</doi></cross_references></HashMap>