SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome.

Subjects

Subjects :

Gene Deletion
Humans
Infant
Mutation
Phenotype
Serine Peptidase Inhibitor Kazal-Type 5 genetics
Netherton Syndrome diagnosis
Netherton Syndrome genetics

Details

Language :

English

ISSN :

1442-200X

Volume :

64

Issue :

1

Database :

MEDLINE

Journal :

Pediatrics international : official journal of the Japan Pediatric Society

Publication Type :

Academic Journal

Accession number :

35438212

Full Text :

https://doi.org/10.1111/ped.15087