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A patient with severe type of epimerase deficiency galactosaemia.
J Inherit Metab Dis. 1988; 11 Suppl 2:249-51.JI

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Authors+Show Affiliations

Sardharwalla IB
Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Manchester, UK.
Wraith JE
No affiliation info available
Bridge C
No affiliation info available
Fowler B
No affiliation info available
Roberts SA
No affiliation info available

MeSH

Carbohydrate EpimerasesFemaleGalactosemiasGalactosephosphatesHumansInfant, NewbornUDPglucose 4-EpimeraseUridine Diphosphate Galactose

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

3141714

Citation

Sardharwalla, I B., et al. "A Patient With Severe Type of Epimerase Deficiency Galactosaemia." Journal of Inherited Metabolic Disease, vol. 11 Suppl 2, 1988, pp. 249-51.
Sardharwalla IB, Wraith JE, Bridge C, et al. A patient with severe type of epimerase deficiency galactosaemia. J Inherit Metab Dis. 1988;11 Suppl 2:249-51.
Sardharwalla, I. B., Wraith, J. E., Bridge, C., Fowler, B., & Roberts, S. A. (1988). A patient with severe type of epimerase deficiency galactosaemia. Journal of Inherited Metabolic Disease, 11 Suppl 2, 249-51.
Sardharwalla IB, et al. A Patient With Severe Type of Epimerase Deficiency Galactosaemia. J Inherit Metab Dis. 1988;11 Suppl 2:249-51. PubMed PMID: 3141714.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A patient with severe type of epimerase deficiency galactosaemia. AU - Sardharwalla,I B, AU - Wraith,J E, AU - Bridge,C, AU - Fowler,B, AU - Roberts,S A, PY - 1988/1/1/pubmed PY - 1988/1/1/medline PY - 1988/1/1/entrez SP - 249 EP - 51 JF - Journal of inherited metabolic disease JO - J Inherit Metab Dis VL - 11 Suppl 2 SN - 0141-8955 UR - https://www.unboundmedicine.com/medline/citation/3141714/A_patient_with_severe_type_of_epimerase_deficiency_galactosaemia_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0141-8955&date=1988&volume=11&issue=&spage=249 DB - PRIME DP - Unbound Medicine ER -