mitochondrial chaperone BCS1 isoform c [Homo sapiens]

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Conformations of Bcs1L undergoing ATP hydrolysis suggest a concerted translocation mechanism for folded iron-sulfur protein substrate. [Nat Commun. 2024]
Conformations of Bcs1L undergoing ATP hydrolysis suggest a concerted translocation mechanism for folded iron-sulfur protein substrate.
Zhan J, Zeher A, Huang R, Tang WK, Jenkins LM, Xia D. Nat Commun. 2024 May 31; 15(1):4655. Epub 2024 May 31.
Expanding the phenotypic spectrum of BCS1L-related mitochondrial disease. [Ann Clin Transl Neurol. 2021]
Expanding the phenotypic spectrum of BCS1L-related mitochondrial disease.
Hikmat O, Isohanni P, Keshavan N, Ferla MP, Fassone E, Abbott MA, Bellusci M, Darin N, Dimmock D, Ghezzi D, et al. Ann Clin Transl Neurol. 2021 Nov; 8(11):2155-2165. Epub 2021 Oct 18.
BCS1L mutations produce Fanconi syndrome with developmental disability. [J Hum Genet. 2022]
BCS1L mutations produce Fanconi syndrome with developmental disability.
Kanako KI, Sakakibara N, Murayama K, Nagatani K, Murata S, Otake A, Koga Y, Suzuki H, Uehara T, Kosaki K, et al. J Hum Genet. 2022 Mar; 67(3):143-148. Epub 2021 Oct 15.

RefSeq genomic sequence
See the genomic reference sequence for the BCS1L gene (NG_033099.2).
RefSeq genomic sequence
See the genomic reference sequence for the BCS1L gene (NG_008018.1).
RefSeq mRNA
See reference mRNA sequence for the BCS1L gene (NM_001371456.1).
RefSeq protein isoforms
See 33 reference sequence protein isoforms for the BCS1L gene.

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