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NG713
NG713
http://dx.doi.org/10.1038/NG713
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome.
P356
Q33954327-96F34B7F-5EFA-4524-850E-330E68199A3F
P356
NG713
http://dx.doi.org/10.1038/NG713