Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene (Q61647740)
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Current Data About Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene
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(P1476) "Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene" (language: en)
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(P2093) Abhimanyu Garg
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Rebecca A Speckman
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(P356) 10.1016/S0002-9343(02)01070-7
(P698) 12015247