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Mariella Granillo-Alvarez
Mariella Granillo-Alvarez
Mexican Social Security Institute
Genetics
Compound heterozygosity
Missense mutation
Haplotype
Stargardt disease
2
Papers
34
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Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome.
2014
Meta Gene
Oscar F. Chacon-Camacho
Rocio Arce-Gonzalez
Vanessa Villegas-Ruiz
E. Pelcastre-Luna
Conrado E. Uría-Gómez
Mariella Granillo-Alvarez
Juan Carlos Zenteno
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Citations (3)
ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation
2013
Experimental Eye Research
Oscar F. Chacon-Camacho
Mariella Granillo-Alvarez
Raul Ayala-Ramirez
Juan Carlos Zenteno
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Citations (31)
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