Novel mutation in Cul7 gene in a family diagnosed with 3M syndrome
dc.contributor.author | Shaikh, S. | |
dc.contributor.author | Shettigar, S. K. G. | |
dc.contributor.author | Santosh Kumar | |
dc.contributor.author | Kantharia, S. | |
dc.date.accessioned | 2020-11-05T05:48:32Z | |
dc.date.available | 2020-11-05T05:48:32Z | |
dc.date.issued | 2019 | |
dc.description.division | MD | en |
dc.format.extent | 4151 bytes | |
dc.format.mimetype | text/html | |
dc.identifier.source | Journal of Genetics, 2019. Vol. 98: Article no. 21 | en |
dc.identifier.uri | http://hdl.handle.net/123456789/21190 | |
dc.language.iso | en | en |
dc.subject | 3M syndrome | en |
dc.subject | ubiquitination | en |
dc.subject | proteasomal degradation | en |
dc.subject | skeletal dysplasia | en |
dc.subject | consanguinity | en |
dc.title | Novel mutation in Cul7 gene in a family diagnosed with 3M syndrome | en |
dc.type | Article | en |