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Description
Mutations in CAV3 can cause a clinical continuum of skeletal muscle phenotypes: limb-girdle muscular dystrophy type 1C (OMIM #607801), rippling muscle disease-2 (OMIM #606072), isolated hyperCKemia (OMIM #123320), and distal myopathy (OMIM #614321) [48]
30 , 31 Prenatal sequencing is possible in the case of maternal MCADD
51% Off 149,00 Alkuperinen hinta oli: 149,00 .105,00 Nykyinen hinta on: 105,00
We found that pre-pregnancy weight and BMI as well as weight gain were significantly different among the four groups with a higher level in the lower FT4level group
