Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: Activity of urea cycle enzymes
- 31 December 1978
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 93 (6) , 986-988
- https://doi.org/10.1016/s0022-3476(78)81230-x
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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- Hyperlysinuria With HyperammonemiaAmerican Journal of Diseases of Children, 1972
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- LOCALISATION OF ENZYMIC DEFECT IN PROPIONICACIDÆMIAThe Lancet, 1970
- Observations on the coexistence of methylmalonic acidemia and glycinemiaThe Journal of Pediatrics, 1969
- Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 PatientsActa Paediatrica, 1967