Molecular characterization of twelve unrelated patients affected by the autosomal recessive osteosclerotic skeletal dysplasia, Pycnodysostosis (cathepsin k deficiency), revealed 11 different genotypes. The mutational profile consisted of 12 different mutations, including nine previously unreported o
Analysis of most common CFTR mutations in patients affected by nasal polyps
β Scribed by Marzena Kostuch; Janusz Klatka; Andrzej Semczuk; Jacek Wojcierowski; Lucas Kulczycki; Jan Oleszczuk
- Book ID
- 106082751
- Publisher
- Springer-Verlag
- Year
- 2005
- Tongue
- English
- Weight
- 235 KB
- Volume
- 262
- Category
- Article
- ISSN
- 0302-9530
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