A. Angius 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.102, pp.713, 2018
Angius, A. Et Al. 2018. Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.. American journal of human genetics , vol.102 , 713.
Angius, A., Uva, P., Buers, I., Oppo, M., Puddu, A., Onano, S., ... Persico, I.(2018). Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.. American journal of human genetics , vol.102, 713.
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.102, 713, 2018
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.102, pp.713, 2018
Angius, A. Et Al. (2018) . "Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.." American journal of human genetics , vol.102, p.713.
@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=2018, pages={713} }