A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
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author: Vera M. Kalscheuer, Jozef Gécz, Cheryl Shoubridge, Stefan Haas, Lachlan A Jolly, Saffron Willis-Owen, Mark A Corbett, Alison Gardner, Anna Hackett, Dagmar Wieczorek, Guy Froyen, Hans-Hilger Ropers
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