Funder
Higher Education Commission, Pakistan
Publisher
Springer Science and Business Media LLC
Reference30 articles.
1. Spritz RA, Chiang PW, Oiso N, Alkhateeb A. Human and mouse disorders of pigmentation. Curr Opin Genet Dev. 2003;13:284–89.
2. Oetting WS, King RA. Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism. Hum Mutat. 1999;13:99–115.
3. Federico JR, Krishnamurthy K. Albinism. [Updated 2018 Oct 27]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2018.
https://www.ncbi.nlm.nih.gov/books/NBK519018/
.
4. Arshad MW, Harlalka GV, Lin S, D’Atri I, Mehmood S, Shakil M, et al. Mutations in TYR and OCA2 associated with oculocutaneous albinism in Pakistani families. Meta Gene. 2018;17:48–55.
5. Lasseaux E, Plaisant C, Michaud V, Pennamen P, Trimouille A, Gaston L, et al. Molecular characterization of a series of 990 index patients with albinism. Pigment Cell Melanoma Res. 2018;31:466–74.
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献