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Genomics of Wolfram Syndrome 1 (WFS1)

Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic atrophy, and deafness and, therefore, is also known as DIDMOAD. Nearly 15,000–30,000 people are affected by WFS worldwide,...

Бүрэн тодорхойлолт

-д хадгалсан:
Номзүйн дэлгэрэнгүй
Үндсэн зохиолч: Sulev Kõks
Формат: Artigo
Хэл сонгох:Inglês
Хэвлэсэн: MDPI AG 2023-09-01
Цуврал:Biomolecules
Нөхцлүүд:
Онлайн хандалт:https://www.mdpi.com/2218-273X/13/9/1346
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