Leber's hereditary optic neuropathy

Ophthalmology Clinics of North America

Volumn 14, Issue 1, 2001, Pages 99-107

  Kerrison, J B ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CENTRAL SCOTOMA; CLINICAL FEATURE; COLOR VISION; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; FAMILY HISTORY; GENETIC DISORDER; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; NEUROLOGIC DISEASE; ONSET AGE; OPTIC NERVE DISEASE; POLYNEUROPATHY; PRIORITY JOURNAL; RETROBULBAR OPTIC NEUROPATHY; REVIEW; SPINOCEREBELLAR DEGENERATION; VISUAL ACUITY; VISUAL FIELD; VISUAL IMPAIRMENT; WOLFRAM SYNDROME; GENETIC LINKAGE; GENETICS; X CHROMOSOME;

DIAGNOSIS, DIFFERENTIAL; GENETIC DISEASES, INBORN; HUMANS; LINKAGE (GENETICS); OPTIC NERVE DISEASES; X CHROMOSOME;

EID: 0035037555     PISSN: 08961549     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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