1H MR spectroscopy of the brain in Cr transporter defect

Molecular Genetics and Metabolism

Volumn 86, Issue 3, 2005, Pages 421-422

  Sijens, P E ^a   Verbruggen, K T ^b   Oudkerk, M ^b   Van Spronsen, F J ^b   Soorani Lunsing, R J ^b  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE; CREATINE PHOSPHATE; GUANIDINOACETIC ACID; METHYLTRANSFERASE; CARRIER PROTEIN; CREATINE TRANSPORTER; DRUG DERIVATIVE; GLYCINE;

BIOSYNTHESIS; BRAIN; CASE REPORT; CREATINE TRANSPORTER DEFECT; ENZYME DEFICIENCY; HUMAN; INBORN ERROR OF METABOLISM; INFANT; LETTER; MALE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTON NUCLEAR MAGNETIC RESONANCE; X CHROMOSOME LINKED DISORDER; GENETICS; METABOLISM; SYNDROME;

BRAIN; CREATINE; GLYCINE; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MALE; MEMBRANE TRANSPORT PROTEINS; SYNDROME;

EID: 27644583776     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2005.08.004     Document Type: Letter

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