ArticleF1000Research2019
Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia.
Jamie Willows et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
3 papers cite it
this papercites it
ArticleF1000Research2019
Jamie Willows et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.