P gene mutations associated with oculocutaneous albinism type II (OCA2)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Cited by 50 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
1. Unsuspected consequences of synonymous and missense variants in OCA2 can be detected in blood cell RNA samples of patients with albinism;Pigment Cell & Melanoma Research;2023-08-31
2. Species differences in hormonally mediated gene expression underlie the evolutionary loss of sexually dimorphic coloration in Sceloporus lizards;Journal of Heredity;2023-07-27
3. Unsuspected consequences of synonymous and missense variants inOCA2can be detected in blood cell RNA samples of patients with albinism;2023-07-09
4. AI-guided cryo-EM probes a thermophilic cell-free system with succinyl-coA manufacturing capability;2022-10-08
5. Clinical and Mutation Spectrum of Autosomal Recessive Non-Syndromic Oculocutaneous Albinism (nsOCA) in Pakistan: A Review;Genes;2022-06-16
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