A. Arlt Et Al. , "Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects," ORPHANET JOURNAL OF RARE DISEASES , vol.17, no.1, 2022
Arlt, A. Et Al. 2022. Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects. ORPHANET JOURNAL OF RARE DISEASES , vol.17, no.1 .
Arlt, A., Kohlschmidt, N., Hentschel, A., Bartels, E., Gross, C., Toepf, A., ... EDEM, P.(2022). Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects. ORPHANET JOURNAL OF RARE DISEASES , vol.17, no.1.
Arlt, Annabelle Et Al. "Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects," ORPHANET JOURNAL OF RARE DISEASES , vol.17, no.1, 2022
Arlt, Annabelle Et Al. "Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects." ORPHANET JOURNAL OF RARE DISEASES , vol.17, no.1, 2022
Arlt, A. Et Al. (2022) . "Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects." ORPHANET JOURNAL OF RARE DISEASES , vol.17, no.1.
@article{article, author={Annabelle Arlt Et Al. }, title={Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects}, journal={ORPHANET JOURNAL OF RARE DISEASES}, year=2022}