G.P.5.10 Novel FHL1 mutation in familial mixed reducing body myopathy with rigid spine

6533b7dbfe1ef96bd1271324

RESEARCH PRODUCT

G.P.5.10 Novel FHL1 mutation in familial mixed reducing body myopathy with rigid spine

Carsten G. Bönnemann Ying Hu Yaqun Zou J. Schessl Thomas Voit Alexandra B. Columbus Hans-hilmar Goebel

subject

medicine.medical_specialty business.industry Rigid spine FHL1 Reducing body myopathy Endocrinology Neurology Internal medicine Pediatrics Perinatology and Child Health Mutation (genetic algorithm)medicine Neurology (clinical)business Genetics (clinical)

year	journal	country	edition	language
2009-09-01	Neuromuscular Disorders

https://doi.org/10.1016/j.nmd.2009.06.088

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