Boyden, L. M. Et Al. 2015. Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia. JOURNAL OF INVESTIGATIVE DERMATOLOGY , vol.135, no.6 , 1540-1547.

Boyden, L. M., Craiglow, B. G., Zhou, J., Hu, R., Loring, E. C., Morel, K. D., ... Lauren, C. T.(2015). Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia. JOURNAL OF INVESTIGATIVE DERMATOLOGY , vol.135, no.6, 1540-1547.

Boyden, Lynn Et Al. "Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia," JOURNAL OF INVESTIGATIVE DERMATOLOGY , vol.135, no.6, 1540-1547, 2015

Boyden, Lynn M. Et Al. "Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia." JOURNAL OF INVESTIGATIVE DERMATOLOGY , vol.135, no.6, pp.1540-1547, 2015

Boyden, L. M. Et Al. (2015) . "Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia." JOURNAL OF INVESTIGATIVE DERMATOLOGY , vol.135, no.6, pp.1540-1547.

@article{article, author={Lynn M. Boyden Et Al. }, title={Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia}, journal={JOURNAL OF INVESTIGATIVE DERMATOLOGY}, year=2015, pages={1540-1547} }