The TGFBI R555W mutation induces a new granular corneal dystrophy type I phenotype

Molecular Vision

Volumn 17, Issue , 2011, Pages 225-230

  Zhu, Yanan ^a   Shentu, Xingchao ^a   Wang, Wei ^a  

^a THE SECOND AFFILIATED HOSPITAL OF ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKERATIN 12; CYTOKERATIN 3;

ARTICLE; CHINESE; CLINICAL ARTICLE; CORNEA DYSTROPHY; EXON; FAMILY STUDY; GENE; GENE MUTATION; GRANULAR CORNEA DYSTROPHY TYPE 1; HETEROZYGOSITY; HUMAN; MISSENSE MUTATION; PEDIGREE; PHENOTYPE; PHOTOPHOBIA; POINT MUTATION; PRIORITY JOURNAL; TRANSFORMING GROWTH FACTOR BETA INDUCED GENE; VISUAL IMPAIRMENT;

CHINA; CORNEAL DYSTROPHIES, HEREDITARY; DNA MUTATIONAL ANALYSIS; EXONS; FAMILY HEALTH; FEMALE; HETEROZYGOTE; HUMANS; MALE; MUTATION; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE; POINT MUTATION; TRANSFORMING GROWTH FACTOR BETA1;

EID: 79551706111     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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