novel mutation

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1
Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population.
Noor, Farjana Akther;Sultana, Nusrat;Bhuyan, Golam Sarower;Islam, Md Tarikul;Hossain, Mohabbat;Sarke...
2020 orphanet journal of rare diseases DOI: 10.1186/s13023-020-1... 237 views
2
Mutations in GAA Gene in Tunisian Families with Infantile Onset Pompe Disease: Novel Mutation and Structural Modeling Investigations.
Alila-Fersi, Olfa;Aloulou, Hajer;Werteni, Ines;Mahfoudh, Nadia;Chabchoub, Imen;Kammoun, Hassen;Keske...
2020 journal of molecular neuroscience : mn DOI: 10.1007/s12031-020-0... 249 views
3
a review on central nervous system effects of gastrodin
;Yuan Liu;Yuan Liu;Jialiang Gao;Min Peng;Hongyan Meng;Hongbo Ma;Pingping Cai;Yuan Xu;Qiong Zhao;Guom...
2018 chemical research in chinese universities DOI: 10.3389/fphar.2018.0... 213 views

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orphanet journal of rare diseases
ISSN: 1750-1172 886 views
journal of molecular neuroscience : mn
ISSN: 1559-1166 354 views

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carrier frequency detection accuracy hrm curve analysis national policy ß-thalassemia founder mutation 3d structure gaa gene infantile pompe disease pharmacokinetics chinese medicine graphene pharmacology dried blood spot optogenetics pharmacology neuropsychiatry biological psychiatry multidrug resistance (mdr)microbiology