A novel mutation I522N within the TGFBI gene caused lattice corneal dystrophy I.

Molecular vision

Volumn 15, Issue , 2009, Pages 2498-2502

  Zhang, Chunmei ^a   Zeng, Guang ^a   Lin, Hui ^a   Li, Dandan ^a   Zhao, Liming ^a   Zhou, Nan ^a   Qi, Yanhua ^a  

^a HARBIN MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BETAIG H3 PROTEIN; BETAIG-H3 PROTEIN; SCLEROPROTEIN; TRANSFORMING GROWTH FACTOR BETA;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CHEMISTRY; CHILD; CONGENITAL CORNEA DYSTROPHY; EXON; FEMALE; GENETICS; HUMAN; MALE; MIDDLE AGED; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BASE SEQUENCE; CHILD; CORNEAL DYSTROPHIES, HEREDITARY; DNA MUTATIONAL ANALYSIS; EXONS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; TRANSFORMING GROWTH FACTOR BETA;

EID: 73449116417     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

References (0)