DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
LinksClose Window
References
Vincent A, Forster N, Maynes JT.
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.
J Med Genet 2014;
51: 797-805
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.