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Showing results 1 to 1 of 1
Title
Author(s)
Issue Date
A recurrent de novo DYNC1H1 tail domain mutation causes spinal muscular atrophy with lower extremity predominance, learning difficulties and mild brain abnormality
Journal:
Neuromuscular Disorders
Chan, HSS
Van Alfen, N
Thuestad, IJ
Ip, J
Chan, AOK
MAK, CCY
Chung, BHY
Aad, VERRIPS
Erik-Jan, KAMSTEEG
2018