Ghosh, S. G. Et Al. 2018. Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS , no.3 , 431-439.

Ghosh, S. G., Becker, K., Huang, H., Salazar, T. D., Chai, G., Salpietro, V., ... Al-Gazali, L.(2018). Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS , no.3, 431-439.

Ghosh, Shereen Et Al. "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome," AMERICAN JOURNAL OF HUMAN GENETICS , no.3, 431-439, 2018

Ghosh, Shereen G. Et Al. "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome." AMERICAN JOURNAL OF HUMAN GENETICS , no.3, pp.431-439, 2018

Ghosh, S. G. Et Al. (2018) . "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome." AMERICAN JOURNAL OF HUMAN GENETICS , no.3, pp.431-439.

@article{article, author={Shereen G. Ghosh Et Al. }, title={Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2018, pages={431-439} }