Cüneyd Yavaş

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 5

Top Topics

Chronic Kidney Disease

Muscular Dystrophy

Top Venues

Genes & genomics

Revista da Associacao Medica Brasileira (1992)

This page only lists publications with an associated author ORCID identifier.

Publications

Cüneyd Yavaş, Mustafa Doğan, Recep Eröz, Kübra Türegün
A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del). Genes & genomics (2024)
Cüneyd Yavaş, Mustafa Doğan, Recep Eröz, Kübra Türegün
A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del). Genes & genomics 46 (5) (2024)
Cüneyd Yavaş, Mustafa Doğan, Recep Eröz, Kübra Türegün
A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del). Genes & genomics 46 (5) (2024)
Cüneyd Yavaş, Mustafa Doğan, Recep Eröz, Kübra Türegün
A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del). Genes & genomics 46 (5) (2024)
Cüneyd Yavaş, Cemal Un, Evrim Çelebi, Alper Gezdirici, Mustafa Doğan, Ezgi Gökpinar İli, Tunay Doğan, Nehir Özdemir Özgentürk
Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome. Revista da Associacao Medica Brasileira (1992) 68 (9) (2022)