unknown [Homo sapiens]

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Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. [J Med Genet. 2016]
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt.
Di Donato N, Neuhann T, Kahlert AK, Klink B, Hackmann K, Neuhann I, Novotna B, Schallner J, Krause C, Glass IA, et al. J Med Genet. 2016 Jun; 53(6):419-25. Epub 2016 Feb 3.
The human v-abl cellular homologue. [J Mol Appl Genet. 1983]
The human v-abl cellular homologue.
Heisterkamp N, Groffen J, Stephenson JR. J Mol Appl Genet. 1983; 2(1):57-68.
The first intron in the human c-abl gene is at least 200 kilobases long and is a target for translocations in chronic myelogenous leukemia. [Mol Cell Biol. 1987]
The first intron in the human c-abl gene is at least 200 kilobases long and is a target for translocations in chronic myelogenous leukemia.
Bernards A, Rubin CM, Westbrook CA, Paskind M, Baltimore D. Mol Cell Biol. 1987 Sep; 7(9):3231-6.

Nucleotide
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Evolutionary Trace of Functional Site [Evolutionary Trace of Functio...]
Evolutionary Trace of Functional Site

LysR substrate-binding domain-containing protein [Aggregatibacter actinomycetemc...
LysR substrate-binding domain-containing protein [Aggregatibacter actinomycetemcomitans]
gi|491742478|ref|WP_005575611.1|

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