Repository of Research and Investigative Information
Baqiyatallah University of Medical Sciences
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(2018) Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy. Oncotarget. pp. 122-141.
(2018) A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing. Bmc Medical Genetics. p. 8. ISSN 1471-2350