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UnknownMECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder.
Not available
S-EPMC5142118 | biostudies-literature
UnknownSUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum.
Not available
S-EPMC9411896 | biostudies-literature
UnknownAssociation of intraoperative end-tidal CO<sub>2</sub> levels with postoperative outcomes: a patient-level analysis of two randomised clinical trials.
Not available
S-EPMC12799414 | biostudies-literature
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