← Evidence map

ArticleBalkan journal of medical genetics : BJMG2018

Myotonic Dystrophy-2: Unusual Phenotype Due to a Small CCTG-expansion.

Finsterer J et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

1 paper cites it

2018
2019
2020
2021
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 30984523