Cite
HARVARD Citation
Ramot, Y. et al. (2014). Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair. Journal of medical genetics. 51 (6), pp. 388-394. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Ramot, Y. et al. (2014). Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair. Journal of medical genetics. 51 (6), pp. 388-394. [Online].