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- [43] Expanding the clinical phenotype of the mitochondrial m.13513G>A mutation with the first report of a fatal neonatal presentation (vol 53, pg 565, 2011) DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2011, 53 (08): : 767 - 767
- [44] Clinical and virological data of the first cases of COVID-19 in Europe: a case series (vol 20, pg 697, 2020) LANCET INFECTIOUS DISEASES, 2020, 20 (06): : E116 - E116
- [45] Clinical and virological data of the first cases of COVID-19 in Europe: a case series (vol 20, pg 697, 2020) LANCET INFECTIOUS DISEASES, 2020, 20 (07): : 148 - 148
- [49] Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome (vol 35, pg 1285, 2014) HUMAN MUTATION, 2015, 36 (02) : 281 - 281