Genomic deletions in <it>OPA1 </it>in Danish patients with autosomal dominant optic atrophy

• Main Authors: Larsen Michael (Author), Milea Dan (Author), Grønskov Karen (Author), Almind Gitte J (Author), Brøndum-Nielsen Karen (Author), Ek Jakob (Author)
• Format: Book
• Published: BMC, 2011-04-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Autosomal dominant optic atrophy (ADOA, Kjer disease, MIM #165500) is the most common form of hereditary optic neuropathy. Mutations in <it>OPA1 </it>located at chromosome 3q28 are the predominant cause for ADOA explainin...