A new type of idiopathic hyperglycinemia with hypo-oxaluria
Pediatrics
.
1965 Dec;36(6):882-91.
Authors
T Gerritsen
,
E Kaveggia
,
H A Waisman
PMID:
5846830
No abstract available
Publication types
Case Reports
MeSH terms
Amino Acid Metabolism, Inborn Errors*
Blood
Cerebrospinal Fluid
Child, Preschool
Chromatography
Glycine / metabolism*
Humans
Infant
Intellectual Disability / etiology
Male
Oxalates / metabolism*
Sweat
Urine
Substances
Oxalates
Glycine