A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations - Concepedia

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A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations

42

Citations

20

References

2010

Year

Dong-Hui Chen, Wendy H. Raskind, William W. Parson, Joshua A. Sonnen, Tiffany Vu, Yunlin Zheng, Mark Matsushita, John Wolff, Hillary Lipe, Thomas D. Bird

Journal of the Neurological Sciences

X-linked Scapuloperoneal MyopathyMendelian DisorderGenetic DisorderMedicineGeneticsPathologyStructural StudyFhl1 MutationsConnective Tissue Disease

References

	Year	Citations

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