Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

M Aminoff, JE Carter, RB Chadwick, C Johnson… - Nature …, 1999 - nature.com
Abstract Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive
disorder characterized by juvenile megaloblastic anaemia, as well as neurological …
被引用次数：322 相关文章
[PDF] academia.edu

[PDF][PDF] Mutations in CUBN, encoding the intrinsic factor-vitamin B 12 receptor, cubilin, cause hereditary megaloblastic anaemia

M Aminoff, JE Carter, RB Chadwick, C Johnson… - nature …, 1999 - academia.edu
Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder
characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that …

[引用][C] Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

M Aminoff, JE Carter, RB Chadwick, C Johnson… - Nature Genetics, 1999 - pure.au.dk
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary
megaloblastic anaemia 1 — Aarhus University Skip to main navigation Skip to search Skip to …
[PDF] researchgate.net

[PDF][PDF] Mutations in CUBN, encoding the intrinsic factor-vitamin B 12 receptor, cubilin, cause hereditary megaloblastic anaemia

M Aminoff, JE Carter, RB Chadwick, C Johnson… - nature …, 1999 - researchgate.net
Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder
characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that …

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.

M Aminoff, JE Carter, RB Chadwick, C Johnson… - Nature …, 1999 - europepmc.org
Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder
characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that …

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

M Aminoff, JE Carter, RB Chadwick… - Nature …, 1999 - mdanderson.elsevierpure.com
Abstract Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive
disorder characterized by juvenile megaloblastic anaemia, as well as neurological …

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

M Aminoff, JE Carter, RB Chadwick… - Nature …, 1999 - ohiostate.elsevierpure.com
Abstract Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive
disorder characterized by juvenile megaloblastic anaemia, as well as neurological …

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

M Aminoff, JE Carter, RB Chadwick… - Nature …, 1999 - pubmed.ncbi.nlm.nih.gov
Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder
characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that …

[引用][C] Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

M AMINOFF, JE CARTER… - Nature …, 1999 - pascal-francis.inist.fr
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause
hereditary megaloblastic anaemia 1 CNRS Inist Pascal-Francis CNRS Pascal and Francis …

Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.

M Aminoff, JE Carter, RB Chadwick… - Nature …, 1999 - search.ebscohost.com
Abstract Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive
disorder characterized by juvenile megaloblastic anaemia, as well as neurological …