 | Up a level |
Bayram, Nurettin 
ORCID: 0000-0003-3244-7328, Kacar Bayram, Ayse, Daimagueler, Hulya-Sevcan, Salimi Dafsari, Hormos ORCID: 0000-0003-3483-5009, Bamborschke, Daniel, Uyanik, Gokhan, Erdogan, Murat, Ozsaygili, Cemal, Pangal, Emine, Yuvaci, Isa, Doganay, Selim, Gumus, Hakan, Per, Huseyin, Jungbluth, Heinz and Cirak, Sebahattin
.
Genotype-phenotype correlations in ocular manifestations of Marinesco-Sjogren syndrome: Case report and literature review.
Eur. J. Ophthalmol..
LONDON:
SAGE PUBLICATIONS LTD.
ISSN 1724-6016
Wang, Haicui, Bayram, Ayse Kacar, Sprute, Rosaenn, Ozdemir, Ozkan, Cooper, Emily, Pergande, Matthias, Efthymiou, Stephanie, Nedic, Ivana, Mazaheri, Neda, Stumpfe, Katharina, Malamiri, Reza Azizi, Shariati, Gholamreza, Zeighami, Jawaher, Bayram, Nurettin, Naghibzadeh, Seyed Kianoosh, Tajik, Mohamad, Yasar, Mehmet, Guven, Ahmet Sami, Bibi, Farah, Sultan, Tipu, Salpietro, Vincenzo, Houlden, Henry, Per, Huseyin, Galehdari, Hamid, Shalbafan, Bita, Jamshidi, Yalda ORCID: 0000-0003-0151-6482 and Cirak, Sebahattin
(2019).
Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking.
Front. Neurosci., 13.
LAUSANNE:
FRONTIERS MEDIA SA.
ISSN 1662-453X
Wang, Haicui, Castiglioni, Claudia ORCID: 0000-0002-1981-7550, Bayram, Ayse Kacar, Fattori, Fabiana ORCID: 0000-0002-1820-8489, Pekuz, Serdar, Araneda, Diego, Per, Huseyin, Erazo, Ricardo, Gumus, Hakan, Zorludemir, Suzan, Becker, Kerstin, Ortega, Ximena, Alfredo Bevilacqua, Jorge, Bertini, Enrico ORCID: 0000-0001-9276-4590 and Cirak, Sebahattin
(2017).
Insights from genotype-phenotype correlations by novel SPEG mutations causing centronuclear myopathy.
Neuromusc. Disord., 27 (9).
S. 836 - 843.
OXFORD:
PERGAMON-ELSEVIER SCIENCE LTD.
ISSN 1873-2364