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Mutations on the Protein: NP_066266 From Positions: 63 To 95

2
0
0
2



OMIM Disease: 118490.0007
p.LEU92PRO
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA


OMIM Disease: 118490.0002
p.PRO93ALA
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA






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