Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient

Molecular Vision

Volumn 16, Issue , 2010, Pages 1570-1575

  Zhang, Bei ^a   Yao, Yu Feng ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CONGO RED; TUMOR ASSOCIATED CALCIUM SIGNAL TRANSDUCER 2; UNCLASSIFIED DRUG;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHINESE; CLINICAL FEATURE; CORNEA DYSTROPHY; DEEP LAMELLAR ENDOTHELIAL KERATOPLASTY; EYE EXAMINATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; KERATECTOMY; MALE; MISSENSE MUTATION; PENETRATING KERATOPLASTY; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RECURRENT DISEASE;

ADOLESCENT; ANTIGENS, NEOPLASM; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CELL ADHESION MOLECULES; CHINA; CODON; CORNEAL DYSTROPHIES, HEREDITARY; DNA MUTATIONAL ANALYSIS; GELATIN; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; RETINAL DEGENERATION; YOUNG ADULT;

EID: 77955600896     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

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