Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. (Q44075701): Difference between revisions
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| 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 | |||||||||||||||
Revision as of 11:42, 11 October 2022
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