Wikidata

(Q38337400)

English

Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.

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title
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
21310915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21310915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
author name string

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