Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. (Q44075701): Difference between revisions
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Jsamwrites (talk | contribs) Updated Item: Added main subject (P921): congenital myopathy (Q112412) with Wikidata:Tools/ItemSubjector (details) |
Changed Asturian description: artículu científicu espublizáu en 2002, bot (details) |
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| description / ast | description / ast | ||||||||||||||
artículu científicu | artículu científicu espublizáu en 2002 | ||||||||||||||
| Property / cites work | |||||||||||||||
| Property / cites work: The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / cites work: The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity / reference | |||||||||||||||
stated in: COCI retrieved: 11 October 2022
reference URL: https://opencitations.net/index/coci/api/v1/citations/10.1126/SCIENCE.280.5360.69 | |||||||||||||||
Latest revision as of 23:22, 19 March 2024
scientific article published in July 2002
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. |
scientific article published in July 2002 |
Statements
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores (English)
C R Müller
B Halliger-Keller
M Brockington
S C Brown
L Feng
A Chattopadhyay
E Mercuri
A Y Manzur
A Ferreiro
N G Laing
M R Davis
H P Roper
V Dubowitz
G Bydder
C A Sewry