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Dfnb59 - Conditional GBA1 deletion model of Type 1 Gaucher Disease: liver and spleen

Annotation:
Dfnb59, deafness, autosomal recessive 59 (human)
Organism:
Mus musculus
Reporter:
GPL6246, 10473089 (ID_REF), GDS4162, NM_001080711, DQ365828, chr2:76650273-76658545 (SPOT ID)
DataSet type:
Expression profiling by array, count, 7 samples

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