Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis
Year: 2009
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddp290
Authors: R. Attali, N. Warwar, A. Israel, I. Gurt, E. McNally, M. Puckelwartz, B. Glick, Y. Nevo, Z. Ben-Neriah, J. Melki
Language: English
Subfield: Developmental Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2106806319