Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism

Celien Grijp, Simon Tavernier, Jana Neirinck, Maha Abdulhadi-Atwan, Julie Van De Velde, Dorien Baetens, Hannah Verdin, Lieve Morbee, Elfride De Baere, David Zangen, Carolien Bonroy, Yolande Van Bever, Hennie Bruggenwirth, Clementien Vermont, Sabine Hannema, Yolanda De Rijke, Petra Schelstraete, Filomeen Haerynck, Martine Cools

Research output: Contribution to journalMeeting AbstractAcademic

Original languageEnglish
Pages (from-to)42-43
JournalHormone Research in Paediatrics
Volume94
Issue numberSUPPL 1
Publication statusPublished - Sep 2021

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