Journal article
Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria
Journal of Medical Genetics, Vol.11(2), pp.121-122
1974
Abstract
Familial cystathioninuria is a rare, hereditary
amino-acid disorder with an autosomal, recessive
pattern of inheritance (Harris, Penrose, and Thomas,
1959; Frimpter, 1972).
Details
- Title
- Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria
- Authors/Creators
- A.H. Bittles (Author/Creator)N.A. Carson (Author/Creator)
- Publication Details
- Journal of Medical Genetics, Vol.11(2), pp.121-122
- Publisher
- BMJ Group
- Identifiers
- 991005540307707891
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
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