Ethiraj Ravindran
3PUBLICATIONS
5CO-AUTHORS
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Publications (3)
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|Dec 13, 2022
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder.Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker
|Jun 25, 2021
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.Ethiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira
|Jun 01, 2021
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.Ethiraj Ravindran, Cynthia Gutierrez de Velazco, Ali Ghazanfar
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