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Long-term Follow-Up of a Patient with Autosomal Dominant Lower Extremity-Predominant Spinal Muscular Atrophy-2 Due to a BICD2 Variant.

Brain and Development(2022)

Cited 0|Views14
Key words
Arthrogryposis multiplex congenital,Lower extremity -predominant spinal muscular atrophy,BICD2
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