document.write("<div class='record'>");
document.write("  <div class='authors'>Heckmann,\&nbsp;K.*\&nbsp;; Iuso,\&nbsp;A.\&nbsp;; Reunert,\&nbsp;J.*\&nbsp;; Grueneberg,\&nbsp;M.*\&nbsp;; Seelhoefer,\&nbsp;A.*\&nbsp;; Rust,\&nbsp;S.*\&nbsp;; Fiermonte,\&nbsp;G.*\&nbsp;; Paradies,\&nbsp;E.*\&nbsp;; Piazzolla,\&nbsp;C.*\&nbsp;; Mannil,\&nbsp;M.*\&nbsp;; Marquardt,\&nbsp;T.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=73410&la=en'>Correction to “Expanding the genetic and clinicalspectrum of SLC25A42 associated disorders and testing ofpantothenic acid to improve CoA level in vitro”.</a></div>");
document.write("  <div class='source'>JIMD Rep. 66:e70002 (2025)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Heckmann,\&nbsp;K.*\&nbsp;; Iuso,\&nbsp;A.\&nbsp;; Reunert,\&nbsp;J.*\&nbsp;; Grüneberg,\&nbsp;M.*\&nbsp;; Seelhöfer,\&nbsp;A.*\&nbsp;; Rust,\&nbsp;S.*\&nbsp;; Fiermonte,\&nbsp;G.*\&nbsp;; Paradies,\&nbsp;E.*\&nbsp;; Piazzolla,\&nbsp;C.*\&nbsp;; Mannil,\&nbsp;M.*\&nbsp;; Marquardt,\&nbsp;T.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=72320&la=en'>Expanding the genetic and clinical spectrum of SLC25A42-associated disorders and testing of pantothenic acid to improve CoA level in vitro.</a></div>");
document.write("  <div class='source'>JIMD Rep. 65, 417-425 (2024)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Della Marina,\&nbsp;A.*\&nbsp;; Leiendecker,\&nbsp;B.*\&nbsp;; Roesch,\&nbsp;S.*\&nbsp;; Wortmann,\&nbsp;S.B.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59091&la=en'>Ketogenic diet for treating alopecia in BCS1l-related mitochondrial disease (Bjornstad syndrome).</a></div>");
document.write("  <div class='source'>JIMD Rep. 53, 10-11 (2020)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Iuso,\&nbsp;A.\&nbsp;; Alhaddad,\&nbsp;B.*\&nbsp;; Weigel,\&nbsp;C.*\&nbsp;; Kotzaeridou,\&nbsp;U.*\&nbsp;; Mastantuono,\&nbsp;E.\&nbsp;; Schwarzmayr,\&nbsp;T.\&nbsp;; Graf,\&nbsp;E.\&nbsp;; Terrile,\&nbsp;C.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Hoffmann,\&nbsp;G.F.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Haack,\&nbsp;T.B.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53683&la=en'>A homozygous splice site mutation in \<em\>SLC25A42\</em\>, encoding the mitochondrial transporter of coenzyme A, causes metabolic crises and epileptic encephalopathy.</a></div>");
document.write("  <div class='source'>JIMD Rep. 44, 1–7 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Thiels,\&nbsp;C.*\&nbsp;; Fleger,\&nbsp;M.*\&nbsp;; Huemer,\&nbsp;M.-T.*\&nbsp;; Rodenburg,\&nbsp;R.J.*\&nbsp;; Vaz,\&nbsp;F.M.*\&nbsp;; Houtkooper,\&nbsp;R.H.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Feichtinger,\&nbsp;R.G.*\&nbsp;; Lücke,\&nbsp;T.*\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Wortmann,\&nbsp;S.B.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47900&la=en'>Atypical clinical presentations of TAZ mutations: An underdiagnosed cause of growth retardation?</a></div>");
document.write("  <div class='source'>JIMD Rep., 89-93 (2016)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Diodato,\&nbsp;D.*\&nbsp;; Invernizzi,\&nbsp;F.*\&nbsp;; Lamantea,\&nbsp;E.*\&nbsp;; Fagiolari,\&nbsp;G.*\&nbsp;; Parini,\&nbsp;R.*\&nbsp;; Menni,\&nbsp;F.*\&nbsp;; Parenti,\&nbsp;G.*\&nbsp;; Bollani,\&nbsp;L.*\&nbsp;; Pasquini,\&nbsp;E.*\&nbsp;; Donati,\&nbsp;M.A.*\&nbsp;; Cassandrini,\&nbsp;D.*\&nbsp;; Santorelli,\&nbsp;F.M.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Ghezzi,\&nbsp;D.*\&nbsp;; Lamperti,\&nbsp;C.*\&nbsp;; Zeviani,\&nbsp;M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31213&la=en'>Common and novel \<em\>TMEM70\</em\> mutations in a cohort of Italian patients with mitochondrial encephalocardiomyopathy.</a></div>");
document.write("  <div class='source'>JIMD Rep. 15, 71-78 (2015)</div>");
document.write("</div>");