A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy.

P C Scacheri; E P Hoffman; J D Fratkin; C Semino-Mora; A Senchak; M R Davis; N G Laing; V Vedanarayanan; S H Subramony

doi:10.1212/wnl.55.11.1689

A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy.

Identifier:nobleid.org/w1/20260515/2FD40B2F

Type:Journal Article

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A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy.

Identifier:nobleid.org/w1/20260515/2FD40B2F

Type:Journal Article

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