Associated Papers
Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children.
Schütz K et al.
Pediatric Pulmonology, 2023
Phenotypic spectrum of FGF10-related disorders: a systematic review.
Bzdega K et al.
Peerj, 2022
Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands.
Seymen F et al.
Clinical Oral Investigations, 2017
Interrogation of a lacrimo-auriculo-dento-digital syndrome protein reveals novel modes of fibroblast growth factor 10 (FGF10) function.
Mikolajczak M et al.
The Biochemical Journal, 2016
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