Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient


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Demir E., Öncül Ü., Havan M., Tuna Kırsaçlıoğlu C., Eminoğlu F. T., Kendirli T., ...Daha Fazla

Clinical Dysmorphology, cilt.32, sa.1, ss.25-28, 2023 (SCI-Expanded) identifier identifier identifier