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Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population
Journal article   Peer reviewed

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

F. Basak Cengiz, Duygu Duman, Aslı Sırmacı, Suna Tokgöz-Yilmaz, Seyra Erbek, Hatice Öztürkmen-Akay, Armaḡan İncesulu, Yvonne J.K Edwards, Hilal Özdaḡ, Xue Z Liu, …
Genetic testing and molecular biomarkers, Vol.14(4), pp.543-550
2010-08
PMID: 20642360

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InCites Highlights

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.150 Hearing Loss
1.150.421 Cochlea
Web Of Science research areas
Biochemistry & Molecular Biology
Genetics & Heredity
ESI research areas
Molecular Biology & Genetics

UN Sustainable Development Goals (SDGs)

This output has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

Source: InCites

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