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
Loss of ninein interferes with osteoclast formation and causes premature ossification.
Gilbert T et al.
Elife, 2024
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
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