Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.

Tanner, Stephan M

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. [electronic resource] - Orphanet journal of rare diseases Aug 2012 - 56 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural

1750-1172

10.1186/1750-1172-7-56 doi


Anemia, Megaloblastic
Ethnicity--genetics
Female
Founder Effect
Genetic Association Studies
Genetic Heterogeneity
Genetic Testing
Humans
Intrinsic Factor--genetics
Malabsorption Syndromes--ethnology
Male
Membrane Proteins
Mutation
Proteins--genetics
Proteinuria--ethnology
Vitamin B 12--metabolism
Vitamin B 12 Deficiency--ethnology