Items where authors include "Carr, I.M."

Article

Harris, E.L., Roy, V., Montagne, M. et al. (15 more authors) (2024) A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes. American Journal of Human Genetics, 111 (1). pp. 119-132. ISSN 0002-9297

Baquero-Perez, B., Antanaviciute, A., Yonchev, I.D. et al. (3 more authors) (2019) The tudor SND1 protein is an m6A RNA reader essential for replication of Kaposi’s sarcoma-associated herpesvirus. eLife, 8. 47261.

Lynex, C.N., Carr, I.M., Leek, J.P. et al. (6 more authors) (2004) Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders. BMC Neurology, 4 (20). ISSN 1471-2377