GUERREIRO, R. J. Et Al. 2013. Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement. JAMA NEUROLOGY , vol.70, no.1 , 78-84.

GUERREIRO, R. J., Lohmann, E., BRAS, J. M., GIBBS, J. R., Rohrer, J. D., Gurunlian, N., ... Dursun, B.(2013). Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement. JAMA NEUROLOGY , vol.70, no.1, 78-84.

GUERREIRO, Rita Et Al. "Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement," JAMA NEUROLOGY , vol.70, no.1, 78-84, 2013

GUERREIRO, Rita J. Et Al. "Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement." JAMA NEUROLOGY , vol.70, no.1, pp.78-84, 2013

GUERREIRO, R. J. Et Al. (2013) . "Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement." JAMA NEUROLOGY , vol.70, no.1, pp.78-84.

@article{article, author={Rita Joao GUERREIRO Et Al. }, title={Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement}, journal={JAMA NEUROLOGY}, year=2013, pages={78-84} }