SPINK5 mutation and FLGgene deletion in an infant with nethertonsyndrome

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Date

2022

Author

Yakut, Tahsin
Karakucak, Mutlu
Ovunc Hacihamdioglu, Duygu
Ferhatoglu, Zeynep Altan
Fisek Izci, Neslihan Muge

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Citation

Hacıhamdioğlu DÖ, Altan Ferhatoğlu Z, Karkucak M, Fişek İzci NM, Yakut T. SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome. Pediatr Int. 2022 Jan;64(1):e15087. doi: 10.1111/ped.15087. PMID: 35438212.

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Source

Pediatrics International

Volume

64

Issue

1

URI

http://doi.org/10.1111/ped.15087
https://hdl.handle.net/20.500.12713/2703

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