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Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria

Bittles, A.H. and Carson, N.A. (1974) Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria. Journal of Medical Genetics, 11 (2). pp. 121-122.

Link to Published Version: http://dx.doi.org/10.1136/jmg.11.2.121
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Abstract

Familial cystathioninuria is a rare, hereditary
amino-acid disorder with an autosomal, recessive
pattern of inheritance (Harris, Penrose, and Thomas,
1959; Frimpter, 1972).

Item Type: Journal Article
Publisher: BMJ Group
URI: http://researchrepository.murdoch.edu.au/id/eprint/12474
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