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
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