Jamal Nasir

2PUBLICATIONS
29CO-AUTHORS
Gene mappingCell and nuclear division
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Publications (2)

|May 08, 2026
The genetic spectrum of achromatopsia in consanguineous families: insights from Whole exome sequencing across 15 affected individuals.

|Jun 21, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.

Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar

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Frequent Collaborators

1 joint publications

Guney Bademci

1 joint publications

María Lachgar-Ruiz

1 joint publications

Mohammad Faraz Zafeer

1 joint publications

Clemer Abad