Torthaí cuardaigh - Boobalan, Elangovan

Two Novel CRX Mutant Proteins Causing Autosomal Dominant Leber Congenital Amaurosis Interact Differently With NRL de réir Nichols, Lorenzo L., Alur, Ramakrishna P., Boobalan, Elangovan, Sergeev, Yuri V., Caruso, Rafael C., Stone, Edwin M., Swaroop, Anand, Johnson, Mary A., Brooks, Brian P.

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Papillorenal Syndrome-Causing Missense Mutations in PAX2/Pax2 Result in Hypomorphic Alleles in Mouse and Human de réir Alur, Ramakrishna P., Vijayasarathy, Camasamudram, Brown, Jacob D., Mehtani, Mohit, Onojafe, Ighovie F., Sergeev, Yuri V., Boobalan, Elangovan, Jones, MaryPat, Tang, Ke, Liu, Haiquan, Xia, Chun-hong, Gong, Xiaohua, Brooks, Brian P.

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Nolz1 expression is required in dopaminergic axon guidance and striatal innervation de réir Soleilhavoup, Clement, Travaglio, Marco, Patrick, Kieran, Garção, Pedro, Boobalan, Elangovan, Adolfs, Youri, Spriggs, Ruth V., Moles-Garcia, Emma, Dhiraj, Dalbir, Oosterveen, Tony, Ferri, Sarah L., Abel, Ted, Brodkin, Edward S., Pasterkamp, R. Jeroen, Brooks, Brian P., Panman, Lia

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