Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia

Annals of Neurology

Volumn 52, Issue 5, 2002, Pages 643-646

  Kure, Shigeo ^a   Kojima, Kanako ^a   Ichinohe, Akiko ^a   Maeda, Tomoki ^b   Kalmanchey, Rozalia ^c   Fekete, György ^c   Berg, Suzan Z ^d   Filiano, Jim ^d   Aoki, Yoko ^a   Suzuki, Yoichi ^a   Izumi, Tatsuro ^b   Matsubara, Yoichi ^a  

^a TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b OITA UNIVERSITY   (Japan)

^c SEMMELWEIS UNIVERSITY OF MEDICINE   (Hungary)

^d DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; FEMALE; GCSH GENE; GENE IDENTIFICATION; GENE MUTATION; GLDC GENE; HETEROZYGOSITY; HUMAN; HYPERGLYCINEMIA; MALE; NEWBORN DISEASE; ONSET AGE; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL;

AMINO ACID OXIDOREDUCTASES; BASE SEQUENCE; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC SCREENING; GLYCINE DEHYDROGENASE; GLYCINE DEHYDROGENASE (DECARBOXYLATING); HETEROZYGOTE; HUMANS; HYPERGLYCINEMIA, NONKETOTIC; INFANT, NEWBORN; MALE; MOLECULAR SEQUENCE DATA; MUTATION;

EID: 0036830348     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10367     Document Type: Article

References (20)

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