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ENCongenital Myopathy 22a, Classic (CMYP22A)
Alias:
Cmyp22a
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Congenital Myopathy 22a, Classic, also known as cmyp22a, is related to myopathy and normokalemic periodic paralysis. An important gene associated with Congenital Myopathy 22a, Classic is SCN4A (Sodium Voltage-Gated Channel Alpha Subunit 4). Affiliated tissues include skeletal muscle and eye, and related phenotypes are ptosis and hypotonia
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MALACARDS
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