| 1 | MGA1, MGA2, AMN, CUBN
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| Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients.
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| Bouchlaka C, Maktouf C, Mahjoub B, Ayadi A, Sfar MT, Sioud M, Gueddich N, Belhadjali Z, Rebai A, Abdelhak S, Dellagi K.
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| J Hum Genet 52(3):262-70. Epub 2007 Feb 7. 2007
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| 2 | MGA1, AMN, CUBN, GIF, MGA2, MGA3
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| Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
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| Tanner SM, Li Z, Perko JD, Oner C, Cetin M, Altay C, Yurtsever Z, David KL, Faivre L, Ismail EA, Grasbeck R, de la Chapelle A.
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| Proc Natl Acad Sci U S A 102(11):4130-3. Epub 2005 Feb 28. 2005
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