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Novel MYO1D Missense Variant Identified Through Whole Exome..:
Alsafwani, Rabab Said
;
Nasser, Khalidah K.
;
Shinawi, Thoraia
...
Frontiers in Medicine. 8 (2021) - p. , 2021
Link:
https://doi.org/10.3389/fmed.2021.724826
RT Journal T1
Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects
UL https://suche.suub.uni-bremen.de/peid=cr-10.3389_fmed.2021.724826&Exemplar=1&LAN=DE A1 Alsafwani, Rabab Said A1 Nasser, Khalidah K. A1 Shinawi, Thoraia A1 Banaganapalli, Babajan A1 ElSokary, Hanan Abdelhalim A1 Zaher, Zhaher F. A1 Shaik, Noor Ahmad A1 Abdelmohsen, Gaser A1 Al-Aama, Jumana Yousuf A1 Shapiro, Adam J. A1 O. Al-Radi, Osman A1 Elango, Ramu A1 Alahmadi, Turki PB Frontiers Media SA YR 2021 SN 2296-858X JF Frontiers in Medicine VO 8 LK http://dx.doi.org/https://doi.org/10.3389/fmed.2021.724826 DO https://doi.org/10.3389/fmed.2021.724826 SF ELIB - SuUB Bremen
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