<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(6)</volume><submitter>Claverie-Martin F</submitter><journal>European journal of human genetics : EJHG</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4795041</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical utility gene card for: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement.</pubmed_title><pmcid>PMC4795041</pmcid><pubmed_authors>Garcia-Nieto V</pubmed_authors><pubmed_authors>Muller D</pubmed_authors><pubmed_authors>Vargas-Poussou R</pubmed_authors><pubmed_authors>Claverie-Martin F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical utility gene card for: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement.</name><description/><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2025-04-05T12:18:49.624Z</modification><creation>2025-04-05T12:18:49.624Z</creation></dates><accession>S-EPMC4795041</accession><cross_references><pubmed>25182135</pubmed><doi>10.1038/ejhg.2014.176</doi></cross_references></HashMap>