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- [31] Carrier frequency of the recurrent mutation c.1643_1644delTG in the XPC gene and birth prevalence of the xeroderma pigmentosum in Morocco JOURNAL OF DERMATOLOGY, 2012, 39 (04): : 382 - 384
- [33] Identification of a novel protein truncating mutation p.Asp98* in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (02):
- [35] Case report: Xeroderma pigmentosum Group A with erythropoietic protoporphyria in a young Chinese patient FRONTIERS IN ENDOCRINOLOGY, 2024, 15
- [37] c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum Archives of Dermatological Research, 2013, 305 : 53 - 57