Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels.-Reference-Cited by-同舟云学术

Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels.

Published:1994-07-01 Issue:7 Volume:31 Page:551-554
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Iolascon A,Parrella T,Perrotta S,Guardamagna O,Coates P M,Sartore M,Surrey S,Fortina P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Acyl CoA dehydrogenase deficiencies;Roe, C.R.; Coates, P.M.,1989

2. Molecular survey of a prevalent mutation, 985A-to-G transition, and identification offive infrequent mutations in the medium-chain acylCoA dehydrogenase gene in 55 patients with mediumchain acyl-CoA dehydrogenase deficiency;Yokota, Y.; Coates, P.M.; Hale, D.E.;Am Hum Genet,1991

3. Mutations in the medium-chain acyl-CoA dehydrogenase gene;Tanaka, K.; Yokota, I.; Coates, P.M.;Hum Mutat,1992

4. Fatty acid oxidation defects as causes of unexpected death in infancy;Bennett, M.J.; Allison, F.; Pollitt, R.J.,1990

5. Medium-chain acylCoA dehydrogenase deficiency: molecular aspects;Matsubara, Y.; Narisawa, K.; Tada, K.;Eur Pediatr,1992

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