Items where Author is "Kamat, MA"

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Journal article

KAMAT, M.A., BACCOLA, A., COOPER, D.N. and CHUZHANOVA, N., 2016. A role for non-B DNA forming sequences in mediating microlesions causing human inherited disease. Human Mutation, 37 (1), pp. 65-73. ISSN 1059-7794

MAYES, M.B., MORGAN, T., WINSTON, J., BUXTON, D.S., KAMAT, M.A., SMITH, D., WILLIAMS, M., MARTIN, R.L., KLEINJAN, D.A., COOPER, D.N., UPADHYAYA, M. and CHUZHANOVA, N., 2015. Remotely acting SMCHD1 gene regulatory elements: in silico prediction and identification of potential regulatory variants in patients with FSHD. Human Genomics, 9. ISSN 1479-7364


KAMAT, M.A., 2014. The involvement of non-B DNA forming sequences in mediating missense mutations, micro-deletions and micro-insertions in human inherited disease. PhD, Nottingham Trent University.

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