Leber’s hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery

Author: Leo-Kottler Beate   Luberichs Janina   Besch Dorothea   Christ-Adler Margot   Fauser Sascha  

Publisher: Springer Publishing Company

ISSN: 0721-832X

Source: Graefe's Archive for Clinical and Experimental Ophthalmology, Vol.240, Iss.9, 2002-09, pp. : 758-764

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content