Corneal dystrophies in Japan

Recent advances in molecular genetics have increased our understanding of the role of genes. Four autosomal dominant corneal dystrophies (CDs); granular CD (GCD), Avellino CD (ACD), lattice CD (LCD), and Reis-Bücklers CD (RBCD) were mapped to the long arm of chromosome 5 (5q31). These four diseases...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of human genetics 2001-01, Vol.46 (8), p.431-435
Hauptverfasser:	Fujiki, K., Nakayasu, K., Kanai, A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Amyloidosis Biomedical and Life Sciences Biomedicine Chromosome 1 Chromosome 5 Chromosomes Codons Cornea Corneal Dystrophies, Hereditary - classification Corneal Dystrophies, Hereditary - genetics Corneal Dystrophies, Hereditary - pathology Corneal dystrophy DNA Mutational Analysis Extracellular Matrix Proteins Gene Expression Gene Function Gene Therapy Genes Genetic Predisposition to Disease - ethnology Genotypes Hereditary diseases Human Genetics Humans Japan - epidemiology mini-review Minireview Missense mutation Molecular Biology Molecular Medicine Mutation Mutation, Missense - genetics Neoplasm Proteins - genetics Phenotypes Polymerase Chain Reaction Surface markers Transforming Growth Factor beta - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!