Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing
Bogusławska, Dżamila M, Skulski, Michał, Machnicka, Beata, Potoczek, Stanisław, Kraszewski, Sebastian, Kuliczkowski, Kazimierz, Sikorski, Aleksander F
Published in International journal of molecular sciences (12.10.2021)
Published in International journal of molecular sciences (12.10.2021)
Get full text
Journal Article
A rare mutation (p.F149del) of the NT5C3A gene is associated with pyrimidine 5'-nucleotidase deficiency
Bogusławska, Dżamila M, Skulski, Michał, Bartoszewski, Rafał, Machnicka, Beata, Heger, Elżbieta, Kuliczkowski, Kazimierz, Sikorski, Aleksander F
Published in Cellular & molecular biology letters (24.11.2022)
Published in Cellular & molecular biology letters (24.11.2022)
Get full text
Journal Article
Efficient method for isolation of reticulocyte RNA from healthy individuals and hemolytic anaemia patients
Skulski, Michał, Bartoszewski, Rafał, Majkowski, Michał, Machnicka, Beata, Kuliczkowski, Kazimierz, Sikorski, Aleksander F., Bogusławska, Dżamila M.
Published in Journal of cellular and molecular medicine (01.01.2019)
Published in Journal of cellular and molecular medicine (01.01.2019)
Get full text
Journal Article
Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing
Bogusławska, Dżamila M, Skulski, Michał, Machnicka, Beata, Potoczek, Stanisław, Kraszewski, Sebastian, Kuliczkowski, Kazimierz, Sikorski, Aleksander F
Published in International journal of molecular sciences (12.10.2021)
Published in International journal of molecular sciences (12.10.2021)
Get full text
Report