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Results: 3

1.

Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency.

Maekawa M, Sudo K, Kanno T, Li SS.

Biochem Biophys Res Commun. 1990 Apr 30;168(2):677-82.

PMID:
2334430
[PubMed - indexed for MEDLINE]
2.

A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes.

Sudo K, Maekawa M, Houki N, Okuda T, Akizuki S, Magara T, Kawano K.

Clin Biochem. 1999 Mar;32(2):137-41. Review.

PMID:
10211631
[PubMed - indexed for MEDLINE]
3.

[Lactate dehydrogenase subunit deficiencies].

Kanno T.

Seikagaku. 1992 Jun;64(6):401-4. Review. Japanese. No abstract available.

PMID:
1506717
[PubMed - indexed for MEDLINE]

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