ADP-ribosylhydrolase like 2 [Rattus norvegicus]

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Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy. [Am J Hum Genet. 2018]
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy.
Danhauser K, Alhaddad B, Makowski C, Piekutowska-Abramczuk D, Syrbe S, Gomez-Ospina N, Manning MA, Kostera-Pruszczyk A, Krahn-Peper C, Berutti R, et al. Am J Hum Genet. 2018 Nov 1; 103(5):817-825. Epub 2018 Oct 25.
Structure-function analyses reveal the mechanism of the ARH3-dependent hydrolysis of ADP-ribosylation. [J Biol Chem. 2018]
Structure-function analyses reveal the mechanism of the ARH3-dependent hydrolysis of ADP-ribosylation.
Wang M, Yuan Z, Xie R, Ma Y, Liu X, Yu X. J Biol Chem. 2018 Sep 14; 293(37):14470-14480. Epub 2018 Jul 25.
Serine ADP-ribosylation reversal by the hydrolase ARH3. [Elife. 2017]
Serine ADP-ribosylation reversal by the hydrolase ARH3.
Fontana P, Bonfiglio JJ, Palazzo L, Bartlett E, Matic I, Ahel I. Elife. 2017 Jun 26; 6. Epub 2017 Jun 26.

RefSeq protein
See the reference protein sequence for ADP-ribosylhydrolase ARH3 (NP_001102150.1).

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Protein