Chattopadhyay, Esita <br/><br/>
A novel mutation at ANTXR1 in an Indian patient with growth retardation-alopecia-pseudoanodontia-optic atrophy syndrome.  [electronic resource] 

 -  Oral surgery, oral medicine, oral pathology and oral radiology  Nov 2017 
 - e261-e265 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>2212-4411 
<br/><br/><label>Standard No.: </label>10.1016/j.oooo.2017.07.009  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alopecia--genetics<br/>Anodontia--genetics<br/>Child<br/>Growth Disorders--genetics<br/>Humans<br/>India<br/>Male<br/>Microfilament Proteins<br/>Mutation--genetics<br/>Neoplasm Proteins--genetics<br/>Optic Atrophies, Hereditary--genetics<br/>Phenotype<br/>Receptors, Cell Surface--genetics