Báo cáo hóa học: " Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations"

Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành hóa học dành cho các bạn yêu hóa học tham khảo đề tài: Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations | Orphanet Journal of Rare Diseases BioMed Central Vz The Open Access Publisher This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text HTML versions will be made available soon. Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia bioinformatic analysis of the protein and predicted effects of all reported mutations Orphanet Journal of Rare Diseases 2012 7 7 doi 1750-1172-7-7 Elisa A Colombo Fernando J Bazan jfbazan@ Gloria Negri Cristina Gervasini Nursel H Elcioglu nelcioglu2@ Deniz Yucelten aysedenizy@ Ilknur Altunay ialtunay@ Umram Cetincelik UCetincelik@ Anna Teti teti@ Andrea Del Fattore Matteo Luciani Spencer K Sullivan SULLIVANSK@ Albert C Yan YANA@ Ludovica Volpi Lidia Larizza ISSN 1750-1172 Article type Research Submission date 6 September 2011 Acceptance date 23 January 2012 Publication date 23 January 2012 Article URL http content 7 1 7 This peer-reviewed article was published immediately upon acceptance. It can be downloaded printed and distributed freely for any purposes see copyright notice below . Articles in Orphanet Journal of Rare Diseases are listed in PubMed and archived at PubMed Central. For information about publishing your research in Orphanet Journal of Rare Diseases or any BioMed 2012 Colombo et al. licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Orphanet Journal of Rare Diseases BioMed Central Vz The Open Access Publisher Central journal go to .

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