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SLC39A10 - Autism, fragile X syndrome, and 15q11-q13 duplication: lymphoblastoid cells

Annotation:
SLC39A10, solute carrier family 39 member 10
Organism:
Homo sapiens
Reporter:
GPL1708, 21925 (ID_REF), GDS2824, NM_020342, A_23_P119778 (SPOT ID)
DataSet type:
Expression profiling by array, log ratio, 30 samples

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