Hereditary deletion of the entireFAM20Cgene in a patient with Raine syndrome

The Raine Syndrome Protein FAM20C Is a Golgi Kinase That Phosphorylates Bio-Mineralization Proteins

(2012) Hiroyuki O. Ishikawa et al.   PLoS One

Secreted Kinase Phosphorylates Extracellular Proteins That Regulate Biomineralization

(2012) V. S. Tagliabracci et al.   SCIENCE

Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice

(2012) Xiaofang Wang et al.   PLoS Genetics

Raine syndrome: a clinical, radiographic and genetic investigation of a case from the Indian subcontinent

(2010) Gurpreet Singh Kochar et al.   CLINICAL DYSMORPHOLOGY

Osteosclerotic bone dysplasia in siblings with a Fam20C mutation

(2010) M Fradin et al.   CLINICAL GENETICS

Raine syndrome: expanding the radiological spectrum

(2010) Mériam Koob et al.   PEDIATRIC RADIOLOGY

Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia

(2009) MA Simpson et al.   CLINICAL GENETICS