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Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria
Journal article   Peer reviewed

Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria

A.H. Bittles and N.A. Carson
Journal of Medical Genetics, Vol.11(2), pp.121-122
1974
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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).

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