Exonal Deletion of SLC24A4 Causes Hypomaturation Amelogenesis Imperfecta

Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta

(2013) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome

(2013) Ken Higashimoto et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

(2012) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Expression of the Sodium/Calcium/Potassium Exchanger, NCKX4, in Ameloblasts

(2012) Ping Hu et al.   CELLS TISSUES ORGANS

Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

(2011) James O'Sullivan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel FAM20A mutations in hypoplastic amelogenesis imperfecta

(2011) Sang Hyun Cho et al.   HUMAN MUTATION

Identification of novel candidate genes involved in mineralization of dental enamel by genome-wide transcript profiling

(2011) Rodrigo S. Lacruz et al.   JOURNAL OF CELLULAR PHYSIOLOGY

The Na+/Ca2+ exchanger NCKX4 governs termination and adaptation of the mammalian olfactory response

(2011) Aaron B Stephan et al.   NATURE NEUROSCIENCE

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

(2009) Walid El-Sayed et al.   AMERICAN JOURNAL OF HUMAN GENETICS

MMP20 Hemopexin Domain Mutation in Amelogenesis Imperfecta

(2009) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

Candidate Gene Strategy Reveals ENAM Mutations

(2009) H.-Y. Kang et al.   JOURNAL OF DENTAL RESEARCH

FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta

(2008) Jung-Wook Kim et al.   AMERICAN JOURNAL OF HUMAN GENETICS