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Number of items: 2.

Journal Article

Karakaya, Mert, Mazaheri, Neda, Polat, Ipek, Bharucha-Goebel, Diana, Donkervoort, Sandra, Maroofian, Reza, Shariati, Gholamreza ORCID: 0000-0002-6295-127X, Hoelker, Irmgard, Monaghan, Kristin, Winchester, Sara, Zori, Robert, Galehdari, Hamid, Bonnemann, Carsten G., Yis, Uluc and Wirth, Brunhilde ORCID: 0000-0003-4051-5191 (2017). Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation. Brain, 140. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Yis, Uluc, Dixit, Vishal, Isikay, Sedat, Karakaya, Mert, Baydan, Figen, Diniz, Gulden, Polat, Ipek, Hiz-Kurul, Semra and Cirak, Sebahattin (2017). Occipital cortex dysgenesis with white matter changes due to mutations in Laminin alpha 2. Turk. J. Pediatr., 59 (3). S. 338 - 342. ANKARA: TURKISH J PEDIATRICS. ISSN 0041-4301

This list was generated on Mon Mar 8 03:26:10 2021 CET.