Publication | Open Access
Myotonic Dystrophy Type 2: Human Founder Haplotype and Evolutionary Conservation of the Repeat Tract
96
Citations
23
References
2003
Year
BiologyRare DiseasesRepeat TractMendelian DisorderGenetic DisorderGeneticsHuman Founder HaplotypeDegenerative DiseaseDisease Gene IdentificationMedicineEvolutionary ConservationClinical Genetics
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