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Ethiraj Ravindran

3PUBLICATIONS
5CO-AUTHORS
Neurology and neuromuscular diseasesMedical infection agents (incl. prions)
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Journal

Publications (3)

Sort by Publication Date:
|Dec 13, 2022
Monoallelic <i>CRMP1</i> 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 <i>MCM7</i> causes autosomal recessive primary microcephaly and intellectual disability.

Ethiraj Ravindran, Cynthia Gutierrez de Velazco, Ali Ghazanfar

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Frequent Collaborators

1 joint publications

Konstantin L Makridis

1 joint publications

Alexander P A Stegmann

1 joint publications

Hao Hu

1 joint publications

Fumio Nakamura

1 joint publications

Angela M Kaindl

Frequent Collaborators

1 joint publications

Konstantin L Makridis

1 joint publications

Alexander P A Stegmann

1 joint publications

Hao Hu

1 joint publications

Fumio Nakamura

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