(Q28295091)

1

0 references

M J Seller

2

0 references

J T Behnam

3

0 references

M A Burdon

4

0 references

D J Spalton

Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects

5

0 references

language of work or name

English

0 references

publication date

January 1999

0 references

published in

Ophthalmology

0 references

volume

106

0 references

issue

1

0 references

page(s)

123-8

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Diagnostic criteria in cominantly inherited juvenile optic atrophy. A report of three new families

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Dominant optic atrophy. The clinical profile

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Autosomal dominant optic atrophy. A spectrum of disability.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

A Clinicopathologic Study of Autosomal Dominant Optic Atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Dominant optic atrophy, Kjer type. Linkage analysis and clinical features in a large British pedigree

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

No evidence of genetic heterogeneity in dominant optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Electrophysiology and colour perimetry in dominant infantile optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Hereditary optic atrophy. An autosomal dominant with incomplete penetrance

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Construction of multilocus genetic linkage maps in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Clinically detectable nerve fiber atrophy precedes the onset of glaucomatous field loss

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Optic nerve damage in human glaucoma. III. Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema, and toxic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021

Visual prognosis in autosomal dominant optic atrophy (Kjer type)

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990013-1

7 January 2021