ArticleOrphanet journal of rare diseases2021
Hearing problems in patients with hereditary gelsolin amyloidosis.
Tuuli Mustonen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
ArticleOrphanet journal of rare diseases2021
Tuuli Mustonen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.