Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case report

Authors

Keywords

Amnionless, Cobalamin deficiency, Anemia, Proteinuria, Vitamin B12, Mutation screening

Journal

Volume 16, Issue 1, Pages -

Publisher

Springer Nature

Online

2015-06-04

DOI

10.1186/s12881-015-0181-2

References

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