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Wided Debbabi

1PUBLICATIONS

1CO-AUTHORS

Paediatrics not elsewhere classified

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Publications (1)

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|May 23, 2022

Fahr syndrome discovered in adulthood revealing a rare <i>GNAS</i> mutation in pseudohypoparathyroidism type 1a in a Tunisian family.

Wided Debbabi, Dayssem Khelifi, Issam Kharrat

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Dayssem Khelifi

Frequent Collaborators

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Dayssem Khelifi

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