De novo SHANK3 mutation causes Rett syndrome‐like phenotype in a female patient
Publisher: John Wiley & Sons Inc
E-ISSN: 1552-4833|167|7|1593-1596
ISSN: 1552-4825
Source: American Journal Of Medical Genetics Part A, Vol.167, Iss.7, 2015-07, pp. : 1593-1596
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Abstract