Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3

American Journal of Ophthalmology

Volumn 130, Issue 4, 2000, Pages 461-468

  Lisch, Walter ^a   Büttner, Andreas ^b   Oeffner, Frank ^c   Böddeker, Inke ^c   Engel, Hartmut ^c   Lisch, Christina ^a   Ziegler, Andreas ^c   Grzeschik, Karl Heinz ^c  

^a City Hospital Hanau   (Germany)

^b Private Practice ^*  (Germany)

^c PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; KERATIN; MICROSATELLITE DNA;

ADULT; AGED; ARTICLE; CHROMOSOME MAP; CHROMOSOME XP; CLINICAL ARTICLE; CONTROLLED STUDY; CORNEA DYSTROPHY; CORNEA EPITHELIUM; FEMALE; GENETIC MARKER; HUMAN; HUMAN CELL; LEUKOCYTE; LISCH CORNEA DYSTROPHY; MALE; MEESMANN CORNEA DYSTROPHY; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE STRAND CONFORMATION POLYMORPHISM; SLIT LAMP; X CHROMOSOME LINKAGE;

ADOLESCENT; ADULT; AGED; CHILD; CHROMOSOME MAPPING; COMPARATIVE STUDY; CORNEAL DYSTROPHIES, HEREDITARY; CORNEAL OPACITY; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; HUMAN; KERATIN; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; MIDDLE AGE; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEX CHROMOSOME ABERRATIONS; X CHROMOSOME;

EID: 0343443045     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(00)00494-3     Document Type: Article

References (13)

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