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

Author:

Sudo Kayoko,Maekawa Masato,Houki Nobuyuki,Okuda Takanari,Akizuki Setsuko,Magara Tadao,Kawano Kazuhiro

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference20 articles.

1. Hereditary deficiency of subunit H of lactate dehydrogenase;Kitamura;Clin Chim Acta,1971

2. A case of deficiency of lactate dehydrogenase H-subunit;Houki;Jpn J Clin Chem,1986

3. Hereditary complete deficiency of lactate dehydrogenase H-subunit;Jyoukyu;Clin Chem,1989

4. A family with a case of deficiency of lactate dehydrogenase H-subunit;Kamada;Seibutsu Butsuri Kagaku,1992

5. Structure of human lactate dehydrogenase-B gene;Takano;Biochem J,1989

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