Wikidata

(Q28296223)

English

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function

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title
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9931337
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9931337%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
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