TY  - GEN
AU  - Akhtar,S
AU  - Bron,A J
AU  - Qin,X
AU  - Creer,R C
AU  - Guggenheim,J A
AU  - Meek,K M
TI  - Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene
SN  - 0950-222X
PY  - 2005///0603
KW  - Amyloid
KW  - analysis
KW  - Antigens, Neoplasm
KW  - genetics
KW  - Base Sequence
KW  - Cell Adhesion Molecules
KW  - Cornea
KW  - chemistry
KW  - Corneal Dystrophies, Hereditary
KW  - Developmental Disabilities
KW  - Extracellular Matrix Proteins
KW  - metabolism
KW  - Female
KW  - Humans
KW  - Infant
KW  - Lactoferrin
KW  - Male
KW  - Microscopy, Immunoelectron
KW  - Pedigree
KW  - Polymorphism, Genetic
KW  - Sequence Analysis, DNA
KW  - Transforming Growth Factor beta
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1038/sj.eye.6701453
ER  -