[PDF][PDF] Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel mutations E176K, W409X and 1223+ 37 del99

V KO, M JANO, J Sokolova, J Oliveriusova, M Orendac… - academia.edu
Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three
novel mutations E176K, W409X and 1223 Page 1 Short Communication Analysis of CBS alleles …

[引用][C] Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel mutations E176K, W409X and 1223+ 37 del99

V Kozich, M Janosík, J Sokolová… - Journal of inherited …, 1997 - pubmed.ncbi.nlm.nih.gov
Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three
novel mutations E176K, W409X and 1223 + 37 del99 Analysis of CBS alleles in Czech and …

[引用][C] Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223+ 37 de199

V Kozich, M Janosik, J Sokolova, J Oliveriusova… - Journal of Inherited …, 1997 - elibrary.ru

[引用][C] Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel mutations E176K, W409X and 1223+ 37 del99.

V Kozich, M Janosík, J Sokolová… - Journal of Inherited …, 1997 - europepmc.org
Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel
mutations E176K, W409X and 1223 + 37 del99. - Abstract - Europe PMC Sign in | Create an …

[引用][C] Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223+ 37 del99

V KOZICH, M JANOSIK, J SOKOLOVA… - Journal of inherited …, 1997 - pascal-francis.inist.fr
Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three
novel mutations E176K, W409X and 1223 + 37 del99 CNRS Inist Pascal-Francis CNRS …

[引用][C] Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223+ 37 del99

V KOZICH, M JANOSIK, J SOKOLOVA… - Journal of inherited …, 1997 - Springer