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NG0695-243
NG0695-243
http://dx.doi.org/10.1038/NG0695-243
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
P356
Q24336919-DFEF453F-2C4B-4623-891F-7C16F0D57B38
P356
NG0695-243
http://dx.doi.org/10.1038/NG0695-243