CBS mutations are good predictors for B6-responsiveness: A study based on the analysis of 35 Brazilian Classical Homocystinuria patients.
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| Abstract | :  Classical homocystinuria (HCU) is a monogenic disease caused by the deficient activity of cystathionine β-synthase (CβS). The objective of this study was to identify the CBS mutations in Brazilian patients with HCU. | 
| Year of Publication | :  2018 | 
| Journal | :  Molecular genetics & genomic medicine | 
| Date Published | :  2018 | 
| URL | :  http://dx.doi.org/10.1002/mgg3.342 | 
| DOI | :  10.1002/mgg3.342 | 
| Short Title | :  Mol Genet Genomic Med | 
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