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INTERNALMEDICINE.9588-17
INTERNALMEDICINE.9588-17
http://dx.doi.org/10.2169/INTERNALMEDICINE.9588-17
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.
P356
Q49963380-22A1FA08-D555-450B-80EC-281B3C240212
P356
INTERNALMEDICINE.9588-17
http://dx.doi.org/10.2169/INTERNALMEDICINE.9588-17