Gelatinous drop-like corneal dystrophy in a child with developmental delay: Clinicopathological features and exclusion of the M1S1 gene

Eye

Volumn 19, Issue 2, 2005, Pages 198-204

  Akhtar, S ^a   Bron, A J ^b   Qin, X ^c   Creer, R C ^a   Guggenheim, J A ^a   Meek, K M ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c SHANDONG UNIVERSITY   (China)

Author keywords

Amyloid; GDLD; Keratoepithelin; M1S1; MAb 5 D 4

Indexed keywords

ADENOSINE; ALANINE; AMYLOID; ASPARTIC ACID; CONGO RED; CYTOSINE; GENOMIC DNA; LACTOFERRIN; PROTEOGLYCAN; SCLEROPROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; BOWMAN MEMBRANE; CASE REPORT; CAUCASIAN; CHROMOSOME BAND; CLINICAL FEATURE; CORNEA DYSTROPHY; CORNEA EPITHELIUM; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DNA EXTRACTION; ELECTRON MICROSCOPY; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; IMMUNOELECTRON MICROSCOPY; KERATOPLASTY; MALE; MOLECULAR GENETICS; MOUTHWASH; NUCLEOTIDE SEQUENCE; RELATIVE; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 14644398011     PISSN: 0950222X     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.eye.6701453     Document Type: Article

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