PTHR1 mutations associated with Ollier disease result in receptor loss of function.
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M. Vikkula | B. Gérard | B. Grandchamp | A. Couvineau | C. Silve | L. Boon | G. Bertrand | V. Wouters | C. Rouyer
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M. Vikkula | B. Gérard | B. Grandchamp | A. Couvineau | C. Silve | L. Boon | G. Bertrand | V. Wouters | C. Rouyer