검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus Goth L, Vitai M, Rass P, Sukei E, Pay A Electrophoresis, 26(9), 1646, 2005 |
| 2 |
A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and Western blot analyses is responsible for the type C of Hungarian acatalasemia Goth L, Rass P, Madarasi I Electrophoresis, 22(1), 49, 2001 |