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1
s12185-012-1100-3
s12185-012-1100-3
https://scigraph.springernature.com/pub.10.1007/s12185-012-1100-3
Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution.
P2888
Q51758787-001D9B98-C293-46C5-AE2A-B98141A3A4E1
P2888
s12185-012-1100-3
https://scigraph.springernature.com/pub.10.1007/s12185-012-1100-3