Publication | Closed Access
(CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients
55
Citations
0
References
1993
Year
Rare DiseasesMendelian DisorderGenetic DisorderTriplet MutationPathologyDegenerative DiseaseDisease Gene IdentificationCommon DiseasesNeuropathologyMedicine
No additional data available for this publication yet. Check back later!