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J.AJHG.2015.01.016
J.AJHG.2015.01.016
http://dx.doi.org/10.1016/J.AJHG.2015.01.016
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.
P356
Q35221418-68F20B95-6BC1-46F0-BB25-A279C4357C89
P356
J.AJHG.2015.01.016
http://dx.doi.org/10.1016/J.AJHG.2015.01.016