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Analysis of novel domain-specific mutations in the zebrafish

Authors :
Ashley N, Turner
Reagan S, Andersen
Ivy E, Bookout
Lauren N, Brashear
James C, Davis
David M, Gahan
John P, Gotham
Baraa A, Hijaz
Ashish S, Kaushik
Jordan B, Mcgill
Victoria L, Miller
Zachariah P, Moseley
Cerissa L, Nowell
Riddhi K, Patel
Mia C, Rodgers
Yazen A, Shihab
Austin P, Walker
Sarah R, Glover
Samantha D, Foster
Anil K, Challa
Source :
Journal of genetics. 97(5)
Publication Year :
2018

Abstract

Nodal-related protein (ndr2) is amember of the transforming growth factor type β superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene encoding nodal cause holoprosencephaly and heterotaxy. Mutations in the

Details

ISSN :
09737731
Volume :
97
Issue :
5
Database :
OpenAIRE
Journal :
Journal of genetics
Accession number :
edsair.pmid..........9bf5e2a2369f51902d41d48e350d19ee