Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.

German journal of ophthalmology

Volumn 5, Issue 4, 1996, Pages 233-240

  Leo Kottler, B ^a   Christ Adler, M ^a   Baumann, B ^a   Zrenner, E ^a   Wissinger, B ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; ELECTRORETINOGRAPHY; EYE FUNDUS; FEMALE; GENETICS; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; METHODOLOGY; MOLECULAR BIOLOGY; OPTIC DISK; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PERIMETRY; POINT MUTATION; POLYMERASE CHAIN REACTION; VISUAL ACUITY; VISUAL FIELD;

ADOLESCENT; ADULT; DNA, MITOCHONDRIAL; ELECTRORETINOGRAPHY; FEMALE; FUNDUS OCULI; HUMANS; MALE; MOLECULAR BIOLOGY; OPTIC ATROPHIES, HEREDITARY; OPTIC DISK; PEDIGREE; PERIMETRY; POINT MUTATION; POLYMERASE CHAIN REACTION; VISUAL ACUITY; VISUAL FIELDS;

EID: 0030183793     PISSN: 09412921     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)