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PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, p. e94960
Journal Article
Journal Article
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by Zhang, Y and Zhang, F and Chen, D and Lü, Q and Tang, L and Yang, C and Lei, M and Tong, N
Brazilian Journal of Medical and Biological Research, ISSN 0100-879X, 2016, Volume 49, Issue 11, p. e5261
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PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, pp. e0124757 - e0124757
Journal Article
FRONTIERS IN NEUROLOGY, ISSN 1664-2295, 11/2018, Volume 9, p. 976
Familial hemiplegic migraine (FHM) is a rare, monogenic, autosomal dominant subtype of migraine, in which three genes, CACNA1A, ATP1A2, and SCN1A, are... 
familial hemiplegic migraine type 3 | migraine | GENE | transient ischemic attack | auras | NEUROSCIENCES | SCN1A mutation | CLINICAL NEUROLOGY | Genetic aspects | Diagnosis | Research | Gene mutations | Migraine
Journal Article
中华医学杂志:英文版, ISSN 0366-6999, 2016, Volume 129, Issue 23, pp. 2810 - 2815
Journal Article
International Journal of Clinical and Experimental Pathology, ISSN 1936-2625, 2017, Volume 10, Issue 6, pp. 6552 - 6559
Objectives: We analyzed gene mutations in a Chinese family with hereditary spherocytosis (HS) combined with glucose-6-phosphate dehydrogenase (G6PD)... 
Glucose-6-phosphate dehydrogenase deficiency | Band 3 | Hemolytic disease | SLC4A1 | Hereditary spherocytosis | DIAGNOSIS | BAND-3 | MEMBRANE | VOLUME | PATHOLOGY | band 3 | FEATURES | HEMOLYTIC-ANEMIA | glucose-6-phosphate dehydrogenase deficiency | ONCOLOGY | THALASSEMIA | UPDATE | MUTATIONS | BINDING | hemolytic disease
Journal Article