Coagulation factor XIII deficiency - Report of a newborn F13A1 Val34Leu polymorphism carrier
Coagulation factor XIII deficiency (FXIIID) is a rare inherited autosomal recessive bleeding disorder. FXIIID is the only coagulation factor deficiency that has been associated with pregnancy loss. Regarding neonates, prolonged umbilical cord bleeding and intracranial hemorrhage, a life-threatening...
Sparad:
Huvudskapare: | , , , , |
---|---|
Materialtyp: | Bok |
Publicerad: |
Hygeia Press di Corridori Marinella,
2022-10-01T00:00:00Z.
|
Ämnen: | |
Länkar: | Connect to this object online. |
Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|
Internet
Connect to this object online.3rd Floor Main Library
Signum: |
A1234.567 |
---|---|
Exemplar 1 | Tillgänglig |