These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
87 related articles for article (PubMed ID: 561525)
41. [Investigative studies on some blinding hereditary eye diseases (author's transl)]. Cao DJ Zhonghua Yan Ke Za Zhi; 1981 Jul; 17(4):233-6. PubMed ID: 6802615 [No Abstract] [Full Text] [Related]
55. [Heredo-familial optic atrophy of a dominant nature. (Clinical study and case report)]. Frasca G; Meduri R; Sighinolfi G Riv Otoneurooftalmol; 1968; 43(1):65-134. PubMed ID: 5704992 [No Abstract] [Full Text] [Related]
56. [Familial incidence of juvenile diabetes mellitus and primary optic atrophy (author's transl)]. Vormittag W; Schwab F; Ferlitsch A Wien Klin Wochenschr; 1978 Jun; 90(13):445-8. PubMed ID: 664711 [TBL] [Abstract][Full Text] [Related]
57. The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype. Rouzier C; Bannwarth S; Chaussenot A; Chevrollier A; Verschueren A; Bonello-Palot N; Fragaki K; Cano A; Pouget J; Pellissier JF; Procaccio V; Chabrol B; Paquis-Flucklinger V Brain; 2012 Jan; 135(Pt 1):23-34. PubMed ID: 22189565 [TBL] [Abstract][Full Text] [Related]
58. [Analysis of Leber's disease in 58 families]. Tong Y Zhonghua Yan Ke Za Zhi; 1985 May; 21(3):163-5. PubMed ID: 3926430 [No Abstract] [Full Text] [Related]
59. [Leber's optic atrophy with a vestibular component. Electronystagmographic study]. Montandon A; Hausler R; Rapp B Rev Otoneuroophtalmol; 1974; 46(5):499-507. PubMed ID: 4549268 [No Abstract] [Full Text] [Related]