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XB-ANAT-1506
Papers associated with skeletal element (and pmp22)
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De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy., Park J., J Med Genet. April 1, 2020; 57 (4): 283-288. |
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Temporal and spatial expression analysis of peripheral myelin protein 22 (Pmp22) in developing Xenopus., Tae HJ., Gene Expr Patterns. January 1, 2015; 17 (1): 26-30.  |
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Mechanisms of amphibian macrophage development: characterization of the Xenopus laevis colony-stimulating factor-1 receptor., Grayfer L., Int J Dev Biol. January 1, 2014; 58 (10-12): 757-66.  |
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Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease., Dubourg O., Brain. October 1, 2001; 124 (Pt 10): 1958-67. |
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Rapid functional analysis in Xenopus oocytes of Po protein adhesive interactions., Yoshida M., Neurochem Res. June 1, 2001; 26 (6): 703-12. |
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