Homo sapiens ferric chelate reductase 1 like (FRRS1L), RefSeqGene on c - Nucleotide

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Movement disorder caused by FRRS1L deficiency may be associated with morphological and functional disorders in Purkinje cells. [Brain Res Bull. 2022]
Movement disorder caused by FRRS1L deficiency may be associated with morphological and functional disorders in Purkinje cells.
Wang R, Liu C, Guo W, Wang L, Chen S, Zhao J, Qin X, Bai W, Yang Z, Kong D, et al. Brain Res Bull. 2022 Dec; 191:93-106. Epub 2022 Oct 27.
Continuous Spikes and Waves During Sleep (CSWS), Severe Epileptic Encephalopathy, and Choreoathetosis due to Mutations in FRRS1L. [Clin EEG Neurosci. 2023]
Continuous Spikes and Waves During Sleep (CSWS), Severe Epileptic Encephalopathy, and Choreoathetosis due to Mutations in FRRS1L.
Mir A, Amer F, Ali M, Alotaibi W, Alotaibi M, Hedaithy A, Aldurayhim F, Hussain F, Bashir S, Housawi Y. Clin EEG Neurosci. 2023 Sep; 54(5):526-533. Epub 2022 Jul 11.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

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Homo sapiens ferric chelate reductase 1 like (FRRS1L), RefSeqGene on chromosome ...
Homo sapiens ferric chelate reductase 1 like (FRRS1L), RefSeqGene on chromosome 9
gi|1047225892|ref|NG_051235.1|

Nucleotide
Gymnura hirundo[orgn] (0)
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