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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

✍ Scribed by Chacón-Camacho, Oscar F.; Granillo-Alvarez, Mariella; Ayala-Ramírez, Raul; Zenteno, Juan C.


Book ID
122802454
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
157 KB
Volume
109
Category
Article
ISSN
0014-4835

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