Decoding Neurologic Disorders with Whole-Genome Sequencing
By Samir Damani
Science Translational Medicine : 23ec42
A next-generation sequencing approach identifies two single nucleotide variants in the gene SH3TCT that contribute to Charcot-Marie-Tooth susceptibility.
Decoding Neurologic Disorders with Whole-Genome Sequencing
By Samir Damani
Science Translational Medicine : 23ec42
A next-generation sequencing approach identifies two single nucleotide variants in the gene SH3TCT that contribute to Charcot-Marie-Tooth susceptibility.