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) |
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| Property / cites work: The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity / rank | |||
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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