Publication | Closed Access
Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum
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Citations
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References
2017
Year
Developmental AnomalyBiallelic MutationsDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsNeuroscienceMedicineEpigeneticsDysmorphic Corpus CallosumDevelopmental Delay
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