13 results on '"Sakai, K."'
Search Results
2. A novel splice site mutation in NCSTN underlies a Japanese family with hidradenitis suppurativa
3. Novel adenosine triphosphate (ATP)–binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
4. microRNA-mediated keratinocyte hyperproliferation in psoriasis vulgaris
5. Partially disturbed lamellar granule secretion in mild congenital ichthyosiform erythroderma with ALOX12B mutations
6. Conradi–Hünermann–Happle syndrome with abnormal lamellar granule contents
7. Novel compound heterozygous nonsense and missense ABCA12 mutations lead to nonbullous congenital ichthyosiform erythroderma
8. Congenital ichthyosiform erythroderma mimicking ichthyosis bullosa of Siemens
9. A novel ABCA12 mutation 3270delT causes harlequin ichthyosis
10. Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: identification of a recurrent p.P25L mutation inKRT5in four affected family members
11. A novel splice site mutation inNCSTNunderlies a Japanese family with hidradenitis suppurativa
12. Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
13. Congenital ichthyosiform erythroderma mimicking ichthyosis bullosa of Siemens
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