Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1

Long-term survival in infantile malignant autosomal recessive osteopetrosis secondary to homozygous p.Arg526Gln mutation in CLCN7

(2012) Piranit Nik Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The V-ATPase a3 subunit mutation R740S is dominant negative and results in osteopetrosis in mice

(2011) Noelle Ochotny et al.   JOURNAL OF BONE AND MINERAL RESEARCH

A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice

(2011) Jennifer A. Calvert et al.   MAMMALIAN GENOME

Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice

(2011) Jennifer M Hilton et al.   GENOME BIOLOGY

Catweasel mice: A novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome

(2009) Erika A. Bosman et al.   DEVELOPMENTAL BIOLOGY

An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda

(2007) Ivana Barbaric et al.   PHYSIOLOGICAL GENOMICS