Autosomal Dominant Hypocalcemia Type 1 and Neonatal Focal Seizures

Autosomal dominant hypocalcemia type 1 (ADH1) is a rare form of hypoparathyroidism that is characterized by gain-of-function mutations in the <i>CASR</i> gene, which provides instructions for producing the protein called calcium-sensing receptor (CaSR). Hypocalcemia in the neonatal perio...

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Bibliographic Details
Main Authors: Raluca Ioana Teleanu (Author), Marlene Alexandra Sarman (Author), Diana Anamaria Epure (Author), Margarita Matei (Author), Ioana Roşca (Author), Eugenia Roza (Author)
Format: Book
Published: MDPI AG, 2023-06-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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