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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Familial case of Blau syndrome associated with a CARD15/NOD2 mutation

Cristina Villanueva-Mendoza1, Lourdes Arellanes-García, Victoria Cubas-Lorenzo

  • 1Asociación para Evitar la Ceguera en México, Genetics, México City, Mexico. villanuevacristina@hotmail.com

Ophthalmic Genetics
|June 23, 2010
PubMed
Abstract

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