Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects

por Alsafwani, Rabab Said, Nasser, Khalidah K., Shinawi, Thoraia, Banaganapalli, Babajan, ElSokary, Hanan Abdelhalim, Zaher, Zhaher F., Shaik, Noor Ahmad, Abdelmohsen, Gaser, Al-Aama, Jumana Yousuf, Shapiro, Adam J., O. Al-Radi, Osman, Elango, Ramu, Alahmadi, Turki
Publicado 2021