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Angelman Syndrome

Angelman syndrome is a rare genetic condition caused by deficient gene expression of E3 ubiquitin protein ligase (also known as UBE3A) and was first described in 1965 by Dr Harry Angelman. Characteristic findings of Angelman syndrome include severe developmental delay and movement or balance disorder, usually in the form of gait ataxia and/or tremulous movement of limbs Join this channel to get access to perks:    / @armandohasudungan   🧠 TEST YOUR KNOWLEDGE FROM THIS LECTURE! ✅ [https://youmakr.ai/test-playground/qu... 👆 Lowkey flex your knowledge. Take the quiz now! Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon:   / armando   👕 Buy shirts: https://teespring.com/stores/ah-7 Social media: 📷 Instagram:   / armandohasudungan   🐦 Twitter:   / armandohasudung   📔 Facebook:   / armandohasudungan   Resources: 📕 Books: http://armandoh.org/resource 🎞️ Equipment: armandoh.org/armando-faigl You can send me mail: 📫 PO BOX 166, Randwick Post Office, Randwick Plaza, NSW 2031, Australia