The Authors Reply

New England Journal of Medicine

Volumn 371, Issue 1, 2014, Pages 82-83

  Mitsui, Jun ^a   Tsuji, Shoji ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; ISOPROTEIN; METHIONINE; UBIDECARENONE; TRANSFERASE;

AMINO ACID SEQUENCE; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; CODON; ENZYME DEFICIENCY; EXON; GENE FREQUENCY; GENETIC TRANSCRIPTION; HUMAN; LETTER; NUCLEOTIDE SEQUENCE; PREVALENCE; PRIORITY JOURNAL; TRANSLATION INITIATION; FEMALE; GENETICS; MALE; NOTE; SHY DRAGER SYNDROME;

ALKYL AND ARYL TRANSFERASES; FEMALE; HUMANS; MALE; MULTIPLE SYSTEM ATROPHY;

EID: 84903717530     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc1311763     Document Type: Letter

References (1)

1. López-Martín JM, Salviati L, Trevisson E, et al. Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis. Hum Mol Genet 2007;16:1091-7. (Pubitemid 47062729)