𝔖 Bobbio Scriptorium
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C.O.4 Dominant mutation in CCDC78 in a unique congenital myopathy with central nuclei and atypical cores

✍ Scribed by Davidson, A.E.; Majczenko, K.; Camelo-Piragua, S.; Li, X.; Joshi, S.; Xu, J.; Peng, W.; Li, J.Z.; Burmeister, M.; Dowling, J.J.


Book ID
119333752
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
49 KB
Volume
22
Category
Article
ISSN
0960-8966

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