Identification of a mutation cluster in mevalonate kinase deficiency, including a new mutation in a patient of Mennonite ancestry
在甲羟戊酸激酶缺乏症中鉴定出一个突变簇,其中包括一名门诺派后裔患者的新突变。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1086/302489
Hinson, D D; Ross, R M; Krisans, S; Shaw, J L; Kozich, V; Rolland, M O; Divry, P; Mancini, J; Hoffmann, G F; Gibson, K M