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In familial cardiac amyloidosis, the amyloid fibrils consist of prealbumin, a mutant of transthyretin.
In familial migraine, the effect size will be high but in sporadic migraine, the effect size will be smaller.
In familial cases, only the proband was analyzed by NGS.
In familial VHL-related RCC, the inheritance pattern is autosomal dominant (Latif et al, 1993).
In familial cases (siblings) where one mutation is found, haplotype analysis (marker analysis) may be recommended.
The findings of this research suggest that the reflexive change in urban families has not resulted in familial individualization.
Severe distraction from interpersonal relationships leading to a negative impact in familial communications was specified by 60 participants.
Genes involved in familial breast cancer, ovarian cancer, and colon cancer have been identified and cloned.
Neuropsychological symptoms are rare in familial hemiplegic migraine (FHM).
A few malignant transformations were reported in familial schwannomatosis [9].
DJ-1 mutations were recently identified in familial PD.
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