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AMMECR1 - Autosomal dominant monocytopenia: polymorphonuclear leukocytes (RNeasy)

Annotation:
AMMECR1, Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Organism:
Homo sapiens
Reporter:
GPL570, 204976_s_at (ID_REF), GDS3819, 9949 (Gene ID), AK023637
DataSet type:
Expression profiling by array, count, 10 samples

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