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  • Id involving MYH6 because possible gene regarding human being ischaemic cardiomyopathy.
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Date Registered:
2025-07-15, 23:30:37
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2025-07-18, 18:33:36
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2025-07-16, 01:27:19
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enotype-phenotype correlation, will further improve detection rates for patients with suspected CMT/HN disorders.
 Severe maternal morbidity (SMM) oc