ŞİMŞEK KİPER, P. Ö. Et Al. 2022. Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3. HUMAN MUTATION , vol.43, no.12 , 2116-2129.

ŞİMŞEK KİPER, P. Ö., Jacob, P., Upadhyai, P., TAŞKIRAN, Z. E., Guleria, V. S., KARAOSMANOĞLU, B., ... İMREN, G.(2022). Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3. HUMAN MUTATION , vol.43, no.12, 2116-2129.

ŞİMŞEK KİPER, PELİN Et Al. "Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3," HUMAN MUTATION , vol.43, no.12, 2116-2129, 2022

ŞİMŞEK KİPER, PELİN Ö. Et Al. "Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3." HUMAN MUTATION , vol.43, no.12, pp.2116-2129, 2022

ŞİMŞEK KİPER, P. Ö. Et Al. (2022) . "Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3." HUMAN MUTATION , vol.43, no.12, pp.2116-2129.

@article{article, author={PELİN ÖZLEM ŞİMŞEK KİPER Et Al. }, title={Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3}, journal={HUMAN MUTATION}, year=2022, pages={2116-2129} }