Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency

Published:1990-08 Issue:1 Volume:171 Page:498-505
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Matsubara Yoichi,Narisawa Kuniaki,Miyabayashi Shigeaki,Tada Keiya,Coates Paul M.,Bachmann Claude,Elsas Louis J.,Pollitt Rodney J.,Rhead William J.,Roe Charles R.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference15 articles.

1. The metabolic basis of inherited disease;Roe,1989

2. The incidence and presentation of dicarboxylic aciduria

3. Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat liver medium chain acyl coenzyme A dehydrogenase.

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