A noncancerous variant of xeroderma pigmentosum type D associated with novel heterozygous missense ERCC2 gene mutation. [electronic resource]
- Indian journal of dermatology, venereology and leprology
- 594-595 p. digital
Publication Type: Case Reports; Letter
0973-3922
10.4103/ijdvl.IJDVL_485_16 doi
Adolescent Child Female Genetic Variation--genetics Heterozygote Humans Male Mutation, Missense--genetics Pedigree Xeroderma Pigmentosum--diagnosis Xeroderma Pigmentosum Group D Protein--genetics