Tags

Type your tag names separated by a space and hit enter

Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation.
Br J Dermatol. 2016 Dec; 175(6):1369-1371.BJ

Authors+Show Affiliations

Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.

Pub Type(s)

Case Reports
Letter

Language

eng

PubMed ID

27106731

Citation

Zhang, J, et al. "Report of a Child With Sporadic Familial Progressive Hyper- and Hypopigmentation Caused By a Novel KITLG Mutation." The British Journal of Dermatology, vol. 175, no. 6, 2016, pp. 1369-1371.
Zhang J, Cheng R, Liang J, et al. Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation. Br J Dermatol. 2016;175(6):1369-1371.
Zhang, J., Cheng, R., Liang, J., Ni, C., Li, M., & Yao, Z. (2016). Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation. The British Journal of Dermatology, 175(6), 1369-1371. https://doi.org/10.1111/bjd.14694
Zhang J, et al. Report of a Child With Sporadic Familial Progressive Hyper- and Hypopigmentation Caused By a Novel KITLG Mutation. Br J Dermatol. 2016;175(6):1369-1371. PubMed PMID: 27106731.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation. AU - Zhang,J, AU - Cheng,R, AU - Liang,J, AU - Ni,C, AU - Li,M, AU - Yao,Z, Y1 - 2016/09/27/ PY - 2016/4/24/pubmed PY - 2017/9/19/medline PY - 2016/4/24/entrez SP - 1369 EP - 1371 JF - The British journal of dermatology JO - Br J Dermatol VL - 175 IS - 6 SN - 1365-2133 UR - https://wwww.unboundmedicine.com/medline/citation/27106731/Report_of_a_child_with_sporadic_familial_progressive_hyper__and_hypopigmentation_caused_by_a_novel_KITLG_mutation_ L2 - https://doi.org/10.1111/bjd.14694 DB - PRIME DP - Unbound Medicine ER -