Corneal Dystrophies, HereditaryCorneal TransplantationFuchs' Endothelial DystrophyCorneal Dystrophy, Juvenile Epithelial of MeesmannCorneaMuscular DystrophiesCollagen Type VIIIEye BanksMyotonic DystrophyDescemet Stripping Endothelial KeratoplastyEndothelium, CornealFetal Tissue TransplantationTissue DonorsEpikeratophakiaStomach UlcerDuodenal UlcerMuscular Dystrophy, DuchenneCorneal DiseasesBrain Tissue TransplantationCorneal OpacityTissue PreservationPedigreeDescemet MembranePeptic UlcerKeratin-12Extracellular Matrix ProteinsBowman MembraneMuscular Dystrophy, AnimalLeg UlcerPressure UlcerKeratoplasty, PenetratingKeratoconusKeratan SulfateSkin UlcerAmyloidosis, FamilialCorneal StromaDNA Mutational AnalysisGraft SurvivalMutationCurrent Procedural TerminologyRetinal DystrophiesCorneal PachymetryPeptic Ulcer HemorrhageDimethylallyltranstransferaseTransforming Growth Factor betaMuscular Dystrophy, FacioscapulohumeralBlood DonorsKeratin-3DystrophinGraft RejectionMutation, MissenseTransplantation, HomologousExonsLiving DonorsTransplantation, HeterologousSulfotransferasesHeterozygotePeptic Ulcer PerforationPhenotypeChromosomes, Human, Pair 5Epithelium, CornealPhotorefractive KeratectomyCorneal EdemaCorneal KeratocytesLasers, ExcimerBuruli UlcerGenes, DominantMuscular Dystrophy, Emery-DreifussMice, Inbred mdxGenetic LinkageEye ProteinsBase SequenceHomozygotePolymerase Chain ReactionMolecular Sequence DataNeuroaxonal DystrophiesChromosomes, Human, Pair 20AmyloidosisSarcoglycansAsian Continental Ancestry GroupCorneal TopographyVisual AcuityMicroscopy, ConfocalAnion Transport ProteinsAmino Acid SubstitutionPoint MutationTransforming Growth Factor beta1ConsanguinityMuscular Dystrophy, OculopharyngealCzech RepublicDystroglycansReflex Sympathetic DystrophyGenetic HeterogeneityFrameshift MutationPolymorphism, Single-Stranded ConformationalGenetic Association StudiesHaplotypesUtrophinVitelliform Macular DystrophyGenotype