المؤلفون: Beech Cameron M, Liyanarachchi Sandya, Shah Nidhi P, Sturm Amy C, Sadiq May F, de la Chapelle Albert, Tanner Stephan M

المصدر: Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 74 (2011)

مصطلحات موضوعية: Imerslund-Gräsbeck syndrome, juvenile cobalamin deficiency, founder mutation, age estimation, mutation screening, anemia, ethnicity, Medicine

Relation: http://www.ojrd.com/content/6/1/74; https://doaj.org/toc/1750-1172; https://doaj.org/article/f1d40d53cdb541e2bc4f3c8bd0fc5e4c

الاتاحة: https://doi.org/10.1186/1750-1172-6-74
https://doaj.org/article/f1d40d53cdb541e2bc4f3c8bd0fc5e4c

المؤلفون: Beech, Cameron M, Liyanarachchi, Sandya, Shah, Nidhi P, Sturm, Amy C, Sadiq, May F, de la Chapelle, Albert, Tanner, Stephan M

مصطلحات موضوعية: Imerslund-Gräsbeck syndrome, juvenile cobalamin deficiency, founder mutation, age estimation, mutation screening, anemia, ethnicity

Relation: http://www.ojrd.com/content/6/1/74

الاتاحة: http://www.ojrd.com/content/6/1/74