Fibrinogen Baltimore I: polymerization defect associated with a gamma 292Gly----Val (GGC----GTC) mutation.

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Article

Fibrinogen Baltimore I: polymerization defect associated with a gamma 292Gly----Val (GGC----GTC) mutation.

Blood - 1 Dec 1990

Bantia S, Mane S M, Bell W R, Dang C V

Abstract excerpt

Fibrinogen Baltimore I is one of the very first congenital abnormal fibrinogens reported over several decades ago; however, the molecular defect of this dysfibrinogen has eluded identification. In fact, several reports misidentified the functional defect of Baltimore I, which has impaired fibrin...

Topics

Adult
Amino Acid Sequence
Base Sequence
Blood Coagulation Disorders
Chromatography, High Pressure Liquid
Codon
Female
Fibrinogens, Abnormal
Fibrinopeptide A
Fibrinopeptide B
Glycine
Humans
Molecular Sequence Data
Mutation
Polymers
Serine Endopeptidases
Valine

Source

Open in PubMed

Identifiers

PMID: 2257302

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-2257302-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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