| scholarly article | Q13442814 |
| P2093 | author name string | C. Raitta | |
| M. Donner | |||
| S. Carlson | |||
| A. W. Eriksson | |||
| E. Vesti | |||
| H. Forsius | |||
| P2860 | cites work | Gyrate atrophy of the choroid and retina: ERG of the neural retina and the pigment epithelium | Q33648091 |
| Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness | Q38671213 | ||
| Corneal wick electrode for recording bright flash electroretinograms and early receptor potentials | Q44427272 | ||
| Aland eye disease (Forsius-Eriksson-Miyake syndrome) with probability established in a Danish family | Q44936014 | ||
| Gene locus for X-linked CSNB | Q68659190 | ||
| A DC electroretinography method for the recording of human a-, b- and c-waves | Q68671441 | ||
| The incremental threshold of the rod visual system and Weber's law | Q69593327 | ||
| The influence of cone adaptation upon rod mediated flicker | Q70159624 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | eye disease | Q3041498 |
| ophthalmology | Q161437 | ||
| P304 | page(s) | 703-710 | |
| P577 | publication date | 1991-12-01 | |
| P1433 | published in | Acta ophthalmologica | Q27708761 |
| P1476 | title | Clinical and electroretinographic comparison between Aland Island eye disease and a newly found related disease with X-chromosomal inheritance | |
| Clinical and electroretinographic comparison between Åland Island eye disease and a newly found related disease with X-chromosomal inheritance | |||
| P478 | volume | 69 |
| Q37312045 | Aland island eye disease: clinical and electrophysiological studies of a Welsh family |
| Q33676559 | Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness |
| Q28214255 | Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina |
| Q24305973 | X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene |
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