LeShon Peart

3PUBLICATIONS
27CO-AUTHORS
Molecular targetsCultural studies of nation and regionNeurology and neuromuscular diseases
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Publications (3)

|Mar 19, 2026
CDK4 and CDK6 variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosis.

Esra Isik, Mohammad Faraz Zafeer, Guney Bademci

|May 03, 2024
Genetic Landscape of Hearing Loss in the Caribbean: A Narrative Review.

LéShon Peart, Mustafa Tekin

|Feb 27, 2024
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.

Marwan Nashabat, Nasrinsadat Nabavizadeh, Hilal Pırıl Saraçoğlu

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Frequent Collaborators

3 joint publications

Mustafa Tekin

1 joint publications

Nasrinsadat Nabavizadeh

1 joint publications

Hilal Pırıl Saraçoğlu

1 joint publications

Burak Sarıbaş