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Introduction: Nonketotic hyperglycinemia (NKH) is a rare disease that is caused by an autosomal recessive congenital error in glycine metabolism. This error causes an accumulation of this amino acid in the body, triggering a series of neurometabolic
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https://explore.openaire.eu/search/publication?articleId=doi_________::4051d88e6fa3c9b542a6188db6959620
Autor:
Soler, Pablo Miralles
Introduction: Nonketotic hyperglycinemia (NKH) is a rare disease that is caused by an autosomal recessive congenital error in glycine metabolism. This error causes an accumulation of this amino acid in the body, triggering a series of neurometabolic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54951b7807d74ad698a1f25329c173de