Angius, A. Et Al. 2016. Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. AMERICAN JOURNAL OF HUMAN GENETICS , vol.99, no.1 , 236-245.

Angius, A., Uva, P., Buers, I., Oppo, M., Puddu, A., Onano, S., ... Persico, I.(2016). Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. AMERICAN JOURNAL OF HUMAN GENETICS , vol.99, no.1, 236-245.

Angius, Andrea Et Al. "Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa," AMERICAN JOURNAL OF HUMAN GENETICS , vol.99, no.1, 236-245, 2016

Angius, Andrea Et Al. "Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa." AMERICAN JOURNAL OF HUMAN GENETICS , vol.99, no.1, pp.236-245, 2016

Angius, A. Et Al. (2016) . "Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa." AMERICAN JOURNAL OF HUMAN GENETICS , vol.99, no.1, pp.236-245.

@article{article, author={Andrea Angius Et Al. }, title={Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2016, pages={236-245} }