Compound heterozygous mutations of the TNXB gene cause primary myopathy - Concepedia

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Compound heterozygous mutations of the TNXB gene cause primary myopathy

41

Citations

21

References

2013

Year

I. Pénisson-Besnier, Valérie Allamand, Philippe Beurrier, Ludovic Martin, Joost Schalkwijk, Ivonne van Vlijmen‐Willems, Corine Gartioux, Fransiska Malfait, Delfien Syx, Laurent Macchi,

Neuromuscular Disorders

Rare DiseasesMendelian DisorderDisease MechanismGenetic DisorderGeneticsPathologyMolecular GeneticsDisease Gene IdentificationCompound Heterozygous MutationsMedicine

References

	Year	Citations

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