Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation
原发性常染色体隐性遗传小头畸形和新型 CDK5RAP2 突变患者的临床和细胞特征
期刊:Orphanet Journal of Rare Diseases
影响因子:3.4
doi:10.1186/1750-1172-8-59
Lina Issa, Katrin Mueller, Katja Seufert, Nadine Kraemer, Henning Rosenkotter, Olaf Ninnemann, Michael Buob, Angela M Kaindl, Deborah J Morris-Rosendahl
