Associated Papers
Expanding the Clinical Phenotype Associated with the NIN Gene; Report of a Patient with Short Stature, Microcephaly and Hearing Loss.
Zamanian Najafabadi S et al.
Archives of Iranian Medicine, 2025
Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein.
Dauber A et al.
The Journal of Clinical Endocrinology and Metabolism, 2012
Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype.
Grosch M et al.
Matrix Biology : Journal of the International Society for Matrix Biology, 0
Select a paper to view details