aprataxin [Rattus norvegicus]

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Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients. [Neurogenetics. 2011]
Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.
Castellotti B, Mariotti C, Rimoldi M, Fancellu R, Plumari M, Caimi S, Uziel G, Nardocci N, Moroni I, Zorzi G, et al. Neurogenetics. 2011 Aug; 12(3):193-201. Epub 2011 Apr 5.
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization. [J Neurol Sci. 2007]
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization.
Ferrarini M, Squintani G, Cavallaro T, Ferrari S, Rizzuto N, Fabrizi GM. J Neurol Sci. 2007 Sep 15; 260(1-2):219-24. Epub 2007 Jun 18.
Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends. [Nucleic Acids Res. 2007]
Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends.
Takahashi T, Tada M, Igarashi S, Koyama A, Date H, Yokoseki A, Shiga A, Yoshida Y, Tsuji S, Nishizawa M, et al. Nucleic Acids Res. 2007; 35(11):3797-809. Epub 2007 May 22.

RefSeq mRNA
See reference mRNA sequence for the Aptx gene (NM_148889.2).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the Aptx gene.

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
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reagents [ExactAntigen/Labome]
reagents
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