Wided Debbabi

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1CO-AUTHORS
Paediatrics not elsewhere classified
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Publications (1)

|May 23, 2022
Fahr syndrome discovered in adulthood revealing a rare GNAS mutation in pseudohypoparathyroidism type 1a in a Tunisian family.

Wided Debbabi, Dayssem Khelifi, Issam Kharrat

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Dayssem Khelifi