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searching for Hereditary elliptocytosis 4 found (25 total)

alternate case: hereditary elliptocytosis

SPTB (1,053 words) [view diff] exact match in snippet view article find links to article

site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain". The Journal

Spectrin, alpha 1 (1,026 words) [view diff] exact match in snippet view article find links to article

type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from

Protein 4.1 (1,332 words) [view diff] exact match in snippet view article find links to article

Ducluzeau MT, Benz EJ, Delaunay J (1992). "Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation

HAGH (817 words) [view diff] exact match in snippet view article find links to article

(1971). "Erythrocyte glyoxalase II deficiency with coincidental hereditary elliptocytosis". Blood. 36 (6): 797–808. doi:10.1182/blood.V36.6.797.797. PMID 5485124