A Rare Cause of Seizures: Hypomagnesemia Type 1

Hypomagnesemia type I is a rare autosomal recessive disorder characterized by severe hypomagnesemia, often accompanied by hypocalcemia. This disease is caused by mutations in the TRPM6 gene (which encodes the respective channel), leading to reduced intestinal absorption of magnesium and increased re...

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Bibliographic Details
Main Authors: Inês Gameiro (Author), Catarina Pinto Silva (Author), Marta Machado (Author), Carolina Cordinhã (Author), Carmen do Carmo (Author), Clara Gomes (Author)
Format: Book
Published: Publicações Ciência e Vida, 2023-12-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available