Geis, T. Et Al. 2019. Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders. ORPHANET JOURNAL OF RARE DISEASES , vol.14 .

Geis, T., Roedl, T., Topaloglu, H., Balci-Hayta, B., Hinreiner, S., Mueller-Felber, W., ... Schoser, B.(2019). Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders. ORPHANET JOURNAL OF RARE DISEASES , vol.14.

Geis, Tobias Et Al. "Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders," ORPHANET JOURNAL OF RARE DISEASES , vol.14, 2019

Geis, Tobias Et Al. "Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders." ORPHANET JOURNAL OF RARE DISEASES , vol.14, 2019

Geis, T. Et Al. (2019) . "Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders." ORPHANET JOURNAL OF RARE DISEASES , vol.14.

@article{article, author={Tobias Geis Et Al. }, title={Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders}, journal={ORPHANET JOURNAL OF RARE DISEASES}, year=2019}