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contentType Journal Article|Research Support, Non-U.S. Gov't
issn 1750-1172
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publicationName Orphanet Journal of Rare Diseases
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bibliographicCitation Corton M, Tatu SD, Avila-Fernandez A, Vallespín E, Tapias I, Cantalapiedra D, Blanco-Kelly F, Riveiro-Alvarez R, Bernal S, García-Sandoval B, Baiget M, Ayuso C. High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population. Orphanet Journal of Rare Diseases. 2013 Feb 05;8(1):20. doi: 10.1186/1750-1172-8-20.
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date 2013-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1186/1750-1172-8-20
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language English
source https://scigraph.springernature.com/
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https://pubmed.ncbi.nlm.nih.gov/
title High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population
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Total number of triples: 44.