Severe form of juvenile corneal stromal dystrophy with homozygous R124H mutation in the keratoepithelin gene in five Japanese patients

AIM—To confirm the mutation of the keratoepithelin gene in patients with a severe form of superficial juvenile granular corneal dystrophy (GCD).
METHODS—Five Japanese probands in whom GCD was diagnosed after histopathological examination and who developed severe manifestations of GCD in their first...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: Mashima, Y., Konishi, M., Nakamura, Y., Imamura, Y., Yamada, M., Ogata, T., Kudoh, J., Shimizu, N.
Format: Artigo
Jezik:Inglês
Izdano: 1998
Teme:
Original articles - Clinical science
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1722402/
https://ncbi.nlm.nih.gov/pubmed/9924333
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items