A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability.
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J. Gécz | S. Haas | H. Ropers | D. Wieczorek | V. Kalscheuer | A. Tzschach | C. Shoubridge | M. Corbett | A. Gardner | A. Hackett | M. Field | L. Jolly | Hao Hu | Monika Y. Cohen | G. Froyen | S. Willis-Owen | Raman Kumar | Evelyn Douglas | Lingli Huang | R. Kumar | M. Cohen | S. Haas