{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,13]],"date-time":"2026-02-13T13:40:17Z","timestamp":1770990017581,"version":"3.50.1"},"reference-count":10,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2016,3,16]],"date-time":"2016-03-16T00:00:00Z","timestamp":1458086400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Case Reports"],"published-print":{"date-parts":[[2016,4]]},"abstract":"<jats:title>Key Clinical Message<\/jats:title><jats:p>Severe recessive mitochondrial myopathy caused by <jats:italic><jats:styled-content style=\"fixed-case\">FBXL<\/jats:styled-content>4<\/jats:italic> gene mutations may present prenatally with polyhydramnios and cerebellar hypoplasia. 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