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A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome

✍ Scribed by Rivera, Henry; Martín-Hernández, Elena; Delmiro, Aitor; García-Silva, María; Quijada-Fraile, Pilar; Muley, Rafael; Arenas, Joaquín; Martín, Miguel A; Martínez-Azorín, Francisco


Book ID
121622506
Publisher
BioMed Central
Year
2013
Tongue
English
Weight
684 KB
Volume
14
Category
Article
ISSN
1471-2369

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