Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing
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Y. Parman | E. Battaloğlu | H. Topaloglu | A. Jordanova | P. De Rijk | A. Estrada-Cuzcano | V. Mitev | I. Tournev | M. Zimon | Daliya Kancheva | D. Atkinson | T. Chamova | A. Yaramis | Gian Maria Fabrizi | Yesim Parma | A. Yaramiş | H. Topaloğlu | Peter De Rijk