A novel mutation at ANTXR1 in an Indian patient with growth retardation-alopecia-pseudoanodontia-optic atrophy syndrome.

Chattopadhyay, Esita

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

Publication Type: Case Reports; Journal Article

2212-4411

10.1016/j.oooo.2017.07.009 doi


Alopecia--genetics
Anodontia--genetics
Child
Growth Disorders--genetics
Humans
India
Male
Microfilament Proteins
Mutation--genetics
Neoplasm Proteins--genetics
Optic Atrophies, Hereditary--genetics
Phenotype
Receptors, Cell Surface--genetics