Add to ORKGAutosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1) (359), is believed to be the most commonof the hereditary optic neuropathies. The estimated disease prevalence is 150,000, or as high as 110,000 inDen mark (360,361)
METHODS: We examined 20 patients from 2 unrelated Swiss families to describe their clinical phenotyp...
Autosomal dominant optic atrophy (OPA, MIM 165500) is an eye disease characterised by variable optic...
Inherited disorders of the optic nerve significantly impact vision in children and adults. The optic...
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1), is believed to ...
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1) (359), is believ...
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1), is believed to ...
Dominant optic atrophy, type Kjer (McKusick no. 165500) is an autosomal dominant eye disease. The di...
"Autosomal dominant optic atrophy (ADOA), or Kjer's disease, often overlaps clinically with other fo...
Here we review how clinically driven research into the basic cellular function of the major determin...
Inherited optic neuropathies are a significant cause of childhood and adult blindness and dominant o...
Dominant optic atrophy (DOA) is the most common hereditary optic neuropathy. The most common form of...
Dominant optic atrophy (DOA) is the commonest form of autosomally-inherited (non-glaucomatous) optic...
1969. Dominant hereditary optic atrophy (Kjer) Pair with IF2_1a. Left eye. Boy with reduced central ...
International audienceDefinition of the disease: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic ...
Aim To review the molecular genetic basis of primary inherited optic neuropathies. Methods Medlin...
METHODS: We examined 20 patients from 2 unrelated Swiss families to describe their clinical phenotyp...
Autosomal dominant optic atrophy (OPA, MIM 165500) is an eye disease characterised by variable optic...
Inherited disorders of the optic nerve significantly impact vision in children and adults. The optic...
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1), is believed to ...
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1) (359), is believ...
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1), is believed to ...
Dominant optic atrophy, type Kjer (McKusick no. 165500) is an autosomal dominant eye disease. The di...
"Autosomal dominant optic atrophy (ADOA), or Kjer's disease, often overlaps clinically with other fo...
Here we review how clinically driven research into the basic cellular function of the major determin...
Inherited optic neuropathies are a significant cause of childhood and adult blindness and dominant o...
Dominant optic atrophy (DOA) is the most common hereditary optic neuropathy. The most common form of...
Dominant optic atrophy (DOA) is the commonest form of autosomally-inherited (non-glaucomatous) optic...
1969. Dominant hereditary optic atrophy (Kjer) Pair with IF2_1a. Left eye. Boy with reduced central ...
International audienceDefinition of the disease: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic ...
Aim To review the molecular genetic basis of primary inherited optic neuropathies. Methods Medlin...
METHODS: We examined 20 patients from 2 unrelated Swiss families to describe their clinical phenotyp...
Autosomal dominant optic atrophy (OPA, MIM 165500) is an eye disease characterised by variable optic...
Inherited disorders of the optic nerve significantly impact vision in children and adults. The optic...