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A rare syndrome: Microcephaly, diabetes mellitus, and epilepsy due to homozygous TRMT10A mutation
Seizure: European Journal of Epilepsy ( IF 3 ) Pub Date : 2024-01-19 , DOI: 10.1016/j.seizure.2024.01.005 Firdevs Ezgi Uçan Tokuç , Meltem Korucuk , Tarkan Kalkan , Fatma Genç
中文翻译:
一种罕见的综合征:TRMT10A 纯合突变导致的小头畸形、糖尿病和癫痫
更新日期:2024-01-19
Seizure: European Journal of Epilepsy ( IF 3 ) Pub Date : 2024-01-19 , DOI: 10.1016/j.seizure.2024.01.005 Firdevs Ezgi Uçan Tokuç , Meltem Korucuk , Tarkan Kalkan , Fatma Genç
中文翻译:
一种罕见的综合征:TRMT10A 纯合突变导致的小头畸形、糖尿病和癫痫