Retinopathy of NARP syndrome

Archives of Ophthalmology

Volumn 118, Issue 2, 2000, Pages 298-299

  Kerrison, John B ^b   Biousse, Valerie ^b   Newman, Nancy J ^a  

^a EMORY EYE CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; CASE REPORT; CLINICAL FEATURE; GENETIC LINKAGE; HUMAN; MUSCLE WEAKNESS; NUCLEIC ACID BASE SUBSTITUTION; OPHTHALMOSCOPY; POINT MUTATION; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SYNDROME;

EID: 0033966108     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.118.2.298     Document Type: Article

References (4)

1. Holt IJ, Harding AE, Petty RKH, et al. A new mitochondrial disease associated with mitochondrial DMA heteroplasmy. Am J Hum Genet. 1990; 46:428-433.
2. Ortiz R, Newman NJ, Shoffner JM, et al. Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation. Arch Ophthalmol. 1993;111:1525-1530.
3. Choweres I, Lerman-Sagie T, Elpeleg ON, Shaag A, Merin S. Cone and rod dysfunction in the NARP syndrome. Br J Ophthalmol. 1999;83:190-193.
4. Weleber RG. Retinitis pigmentosa and allied disorders. In:Retina. St Louis, Mo: Mosby-YearBook Inc; 1994:341-350. Ryan SJ, Ogden TE, eds. Basic Science and Inherited Retinal Disease, vol 1, 2nd ed.