17695617 - GEO Profiles - NCBI

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Fibcd1 - Werner syndrome protein and poly(ADP-ribose) polymerase-1 null mutants

Annotation:: Fibcd1, fibrinogen C domain containing 1

Organism:: Mus musculus

Reporter:: GPL891, 10217 (ID_REF), GDS1675, NM_178887, A_51_P271417 (SPOT ID)

DataSet type:: Expression profiling by array, log ratio, 6 samples

ID:: 17695617

GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors

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Optic Atrophies, Hereditary
Optic Atrophies, Hereditary
Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, ...<br/>Year introduced: 2000(1989)

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