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Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.

Annals of hematology - 1 Dec 2017

Kedar Prabhakar, Parmar Vaishali, Devendra Rati, Gupta Vinod, Warang Prashant, Madkaikar Manisha

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Share to Amino Acid Substitution
Share to Anemia, Dyserythropoietic, Congenital
Share to Consanguinity
Share to Diagnostic Errors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Mutation, Missense

Share to Spherocytosis, Hereditary

Share to Vesicular Transport Proteins

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Identifiers

PMID: 28879554
DOI: 10.1007/s00277-017-3116-5

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Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.PMID 28879554Read ↗

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