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Q45858519-617A4281-3ECF-47BD-B294-EF2FA6850A3A
Q45858519-617A4281-3ECF-47BD-B294-EF2FA6850A3A
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Statement
http://www.wikidata.org/entity/statement/Q45858519-617A4281-3ECF-47BD-B294-EF2FA6850A3A
Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.
P2860
Q45858519-617A4281-3ECF-47BD-B294-EF2FA6850A3A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45858519-617A4281-3ECF-47BD-B294-EF2FA6850A3A
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wasDerivedFrom
3fc5ddfda9cd131cfce205b6fbc84257c5174fda
P2860
An update of the mutation profile of Factor 13 A and B genes.