Vocal cord paralysis in autosomal dominant spinal muscular atrophy due to BICD2

Congenit Anom (Kyoto). 2023 Mar;63(2):52-53. doi: 10.1111/cga.12500. Epub 2022 Dec 20.

Authors

Sachiko Matsui¹, Sota Iwatani¹, Naoya Morisada², Toshiki Takenouchi³, Seiji Yoshimoto¹

Affiliations

¹ Department of Neonatology, Hyogo Prefectural Kobe Children's Hospital, Kobe, Hyogo, Japan.
² Department of Clinical Genetics, Hyogo Prefectural Kobe Children's Hospital, Kobe, Hyogo, Japan.
³ Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.

PMID: 36517450
DOI: 10.1111/cga.12500

No abstract available

MeSH terms

Humans
Microtubule-Associated Proteins
Muscular Atrophy, Spinal*
Vocal Cord Paralysis*

Substances

BICD2 protein, human
Microtubule-Associated Proteins

Grants and funding

JP22gk0110038/Japan Agency for Medical Research and Development