Bmpr1aa modulates the severity of the skeletal phenotype in an fkbp10-deficient Bruck syndrome zebrafish model.

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DOI:10.1093/jbmr/zjae185
作者：Tamara Jarayseh,?Sophie Debaenst,?Hanna De Saffel,?Toon Rosseel,?Mauro Milazzo,?Jan Willem Bek,?David M Hudson,?Filip Van Nieuwerburgh,?Yannick Gansemans,?Iván Josipovic,?Matthieu N Boone,?P Eckhard
文献类型：期刊论文
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Oxford University Press

Abstract：Rare monogenic disorders often exhibit significant phenotypic variability among individuals sharing identical genetic mutations. Bruck syndrome (BS), a prime example, is characterized by bon

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