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Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4

机译：鉴定受异常OCA 4型影响的匈牙利谱系中SLC45A2基因的两个新突变

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Tóth Lola; Fábos Beáta; Farkas Katalin; Sulák Adrienn; Tripolszki Kornélia; Széll Márta; Nagy Nikoletta;
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1. Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4 [J] . Lola Tóth, Beáta Fábos, Katalin Farkas, BMC Medical Genetics . 2017,第1期

机译：鉴定受异常OCA 4型影响的匈牙利谱系中SLC45A2基因的两个新突变
2. Mutational Analysis of TYR , OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism [J] . Ye Lin, Xihui Chen, Ying Yang, Molecular Genetics & Genomic Medicine . 2019,第7期

机译：血管皮内常杂化的中国家庭中TYR，OCA2和SLC45A2基因的突变分析
3. Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree [J] . HawkesJ.E., CassidyP.B., MangaP., Journal of dermatological science . 2013,第1期

机译：家族性黑色素瘤谱系中新型OCA2基因突变的报道和OCA2变体对黑色素瘤风险的研究
4. Identification of gene signature associated with type 2 diabetes mellitus by integrating mutation and expression data* [C] . Zijun Zhu, Xudong Han, Liang Cheng IEEE International Conference on Bioinformatics and Biomedicine . 2020

机译：通过整合突变和表达数据鉴定与2型糖尿病患者的基因签名*
5. Conditional linkage methods--Searching for modifier genes in a large Amish pedigree with known von Willebrand Disease major gene mutation. [D] . Abbott, Diana Lee. 2009

机译：条件连锁法-在一个大型阿米什（Amish）谱系中搜索具有已知von Willebrand疾病主要基因突变的修饰基因。
6. Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4 [O] . Lola Tóth, Beáta Fábos, Katalin Farkas, 2017

机译：鉴定受异常OCA 4型影响的匈牙利谱系中SLC45A2基因的两个新突变
7. Identification of Two Novel Mutations in the SLC45A2 Gene in a Hungarian Pedigree Affected by Unusual OCA Type 4 [O] . Tóth L, Fábos B 2015

机译：鉴定受异常OCA型匈牙利血统中SLC45A2基因的两种新突变

Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4

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