FARSLA [Homo sapiens]

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FARSA mutations mimic phenylalanyl-tRNA synthetase deficiency caused by FARSB defects. [Clin Genet. 2019]
FARSA mutations mimic phenylalanyl-tRNA synthetase deficiency caused by FARSB defects.
Krenke K, Szczałuba K, Bielecka T, Rydzanicz M, Lange J, Koppolu A, Płoski R. Clin Genet. 2019 Nov; 96(5):468-472. Epub 2019 Aug 6.
Compound heterozygosity for loss-of-function FARSB variants in a patient with classic features of recessive aminoacyl-tRNA synthetase-related disease. [Hum Mutat. 2018]
Compound heterozygosity for loss-of-function FARSB variants in a patient with classic features of recessive aminoacyl-tRNA synthetase-related disease.
Antonellis A, Oprescu SN, Griffin LB, Heider A, Amalfitano A, Innis JW. Hum Mutat. 2018 Jun; 39(6):834-840. Epub 2018 Apr 10.
Cloning and expression of human phenylalanyl-tRNA synthetase in Escherichia coli: comparative study of purified recombinant enzymes. [Protein Expr Purif. 2002]
Cloning and expression of human phenylalanyl-tRNA synthetase in Escherichia coli: comparative study of purified recombinant enzymes.
Moor N, Linshiz G, Safro M. Protein Expr Purif. 2002 Mar; 24(2):260-7.

RefSeq protein
See the reference protein sequence for phenylalanine--tRNA ligase alpha subunit (NP_004452.1).

Nucleotide
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FARSLA [Homo sapiens]
FARSLA [Homo sapiens]
gi|48145597|emb|CAG33021.1|

Protein

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Protein