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Primigravida with Bernard-Soulier Syndrome: a case report
BACKGROUND: Bernard-Soulier Syndrome is a rare congenital bleeding disorder, mainly inherited in an autosomal recessive pattern. It is characterized by a genetic defect on one of the four genes encoding the subunits of the transmembrane protein complex GPIb-V-IX, physiologically expressed only in pl...
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| Pubblicato in: | BMC Res Notes |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4434533/ https://ncbi.nlm.nih.gov/pubmed/25928053 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1145-5 |
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