A case of congenital myopathy accompanied by tremor due to a MYBPC1 mutation. Issue 1 (5th May 2022)
- Record Type:
- Journal Article
- Title:
- A case of congenital myopathy accompanied by tremor due to a MYBPC1 mutation. Issue 1 (5th May 2022)
- Main Title:
- A case of congenital myopathy accompanied by tremor due to a MYBPC1 mutation
- Authors:
- Shiraishi, Kazuhiro
Tsuburaya, Rie S
Mukaida, Shoichi
Yano, Naoko
Yoshida, Takeshi - Abstract:
- Is Part Of:
- Pediatrics international. Volume 64:Issue 1(2022)
- Journal:
- Pediatrics international
- Issue:
- Volume 64:Issue 1(2022)
- Issue Display:
- Volume 64, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 64
- Issue:
- 1
- Issue Sort Value:
- 2022-0064-0001-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-05-05
- Subjects:
- congenital myopathy -- MYOTREM -- slow skeletal isoform of myosin binding protein C gene (MYBPC1) -- tremor -- whole exome sequencing
Pediatrics -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1442-200X/issues. Subscription to online journal required for access to full text. ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ped.15061 ↗
- Languages:
- English
- ISSNs:
- 1328-8067
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.655800
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25607.xml