Wikidata

(Q45865748)

English

Identification of CNGA3 mutations in 46 families: common cause of achromatopsia and cone-rod dystrophies in Chinese patients

scientific article published in September 2014

In more languages

Statements

title
Identification of CNGA3 mutations in 46 families: common cause of achromatopsia and cone-rod dystrophies in Chinese patients (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24903488
retrieved
17 December 2017
reference URL
http://europepmc.org/abstract/MED/24903488

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