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متن کاملProceedings of the 2nd BEAT-PCD Conference and 3rd PCD training School: part 2
Primary ciliary dyskinesia is a rare, autosomal recessive genetic based disease causing functional and/or structural defects of cilia. However, there are little information about the genetic basis of this disease. By this time, we know that, mutations on the DNAI1 and DNA5H genes are responsible for encoding of dynein proteins of cilia, causing this disorder. Discrimination of the PCD from othe...
متن کاملProceedings of the 2nd BEAT-PCD conference and 3rd PCD training school: part 1
Primary ciliary dyskinesia (PCD) is a rare heterogenous condition that causes progressive suppurative lung disease, chronic rhinosinusitis, chronic otitis media, infertility and abnormal situs. ‘Better Experimental Approaches to Treat Primary Ciliary Dyskinesia’ (BEAT-PCD) is a network of scientists and clinicians coordinating research from basic science through to clinical care with the intent...
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ژورنال
عنوان ژورنال: Physics Procedia
سال: 2014
ISSN: 1875-3892
DOI: 10.1016/j.phpro.2014.08.024