has been cited by the following article(s):
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[1]
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Fahr syndrome discovered in adulthood revealing a rare
GNAS
mutation in pseudohypoparathyroidism type 1a in a Tunisian family
Clinical Case Reports,
2022
DOI:10.1002/ccr3.5849
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[2]
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Fahr syndrome discovered in adulthood revealing a rare GNAS mutation in pseudohypoparathyroidism type 1a in a Tunisian family
Clinical Case Reports,
2022
DOI:10.1002/ccr3.5849
|
|
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