TY  - GEN
AU  - Tanner,Stephan M
AU  - Li,Zhongyuan
AU  - Perko,James D
AU  - Oner,Cihan
AU  - Cetin,Mualla
AU  - Altay,Cigdem
AU  - Yurtsever,Zekiye
AU  - David,Karen L
AU  - Faivre,Laurence
AU  - Ismail,Essam A
AU  - Gräsbeck,Ralph
AU  - de la Chapelle,Albert
TI  - Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene
SN  - 0027-8424
PY  - 2005///0509
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 11
KW  - Female
KW  - Humans
KW  - Intrinsic Factor
KW  - genetics
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Vitamin B 12
KW  - metabolism
KW  - Vitamin B 12 Deficiency
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1073/pnas.0500517102
ER  -