TableĀ 1.

Human diseases caused by mutation of Golgi-localised proteins where a major aspect of the disease phenotype is due to an impairment of ECM assembly or function

Human diseases caused by mutation of Golgi-localised proteins where a major aspect of the disease phenotype is due to an impairment of ECM assembly or function
Human diseases caused by mutation of Golgi-localised proteins where a major aspect of the disease phenotype is due to an impairment of ECM assembly or function
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