Aldolase Activity in the Plasma or Serum of Normal Children and Families with Muscular Dystrophy

Author:

Clayton B. E.,Wilson K. M.,Carter C. O.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Progressive muscular dystrophy. II. Biochemical identification of the carrier state in the recessive sex-linked juvenile (Duchenne) type by serum creatine-phosphokinase determinations;Aebi, U.; Richterich, R.; Colombo, J.P.; Rossi, E.;Enzym. biol. clin,1961

2. Zur Genetik der Myopathien;Becker, P.E.;Dtsch. Z. Nervenheilk,1955

3. Muscular dystrophy in childhood. The genetic aspect. A field study in the Leeds region of clinical types and their inheritance;Blyth, H.; Pugh, R.J.;Ann hum. Genet,1959

4. Serum enzymes and genetic carriers in muscular dystrophy;Chung, C.S.; Morton, N.E.; Peters, H.A.;Amer. J. hum. Genet,1960

5. Serum aldolase and the diagnosis of myopathy;Evans, J.H.; Baker, R.W.R.;Brain,1957

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