Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

Journal of Inherited Metabolic Disease

Volumn 24, Issue 4, 2001, Pages 448-464

  Mudd, S H ^a   Cerone, R ^e   Schiaffino, M C ^e   Fantasia, A R ^e   Minniti, G ^e   Caruso, U ^e   Lorini, R ^e   Watkins, D ^f   Matiaszuk, N ^f   Rosenblatt, D S ^f   Schwahn, B ^f   Rozen, R ^f   LeGros, L ^g   Kotb, M ^g   Capdevila, A ^h   Luka, Z ^h   Finkelstein, J D ⁱ   Tangerman, A ^b   Stabler, S P ^c   Allen, R H ^c   Wagner, C ^d   more..

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF COLORADO   (United States)

^d VETERANS AFFAIRS MEDICAL CENTER   (United States)

^e G GASLINI INSTITUTE   (Italy)

^f MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^g UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^h VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

ⁱ GEORGE WASHINGTON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; CYSTATHIONINE BETA SYNTHASE; GLYCINE METHYLTRANSFERASE; METHIONINE; METHIONINE ADENOSYLTRANSFERASE; METHYLTRANSFERASE; S ADENOSYLMETHIONINE; SARCOSINE; UNCLASSIFIED DRUG;

ALANINE AMINOTRANSFERASE BLOOD LEVEL; AMINO ACID BLOOD LEVEL; AMINOACIDEMIA; ARTICLE; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; CASE REPORT; CHILD; CLINICAL FEATURE; ENZYME DEFICIENCY; FEMALE; GLYCINE N METHYLTRANSFERASE DEFICIENCY; HEPATOMEGALY; HUMAN; HYPERMETHIONINEMIA; INBORN ERROR OF METABOLISM; LABORATORY TEST; LIVER DISEASE; MALE; SIBLING; TYROSINEMIA; ULTRASOUND;

ALANINE TRANSAMINASE; ASPARTATE AMINOTRANSFERASES; CHILD; CHILD, PRESCHOOL; DIET; FEMALE; GLYCINE N-METHYLTRANSFERASE; HEPATOMEGALY; HUMANS; LIVER; METHIONINE; METHYLTRANSFERASES; S-ADENOSYLMETHIONINE; SARCOSINE;

EID: 0034827802     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1010577512912     Document Type: Article

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