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A further analysis showed however that spouses of MO probands have 1.4 times the risk of MO, and spouses of MA probands have no increased risk of MA [3], thus backing a hereditary liability for MO and especially MA.
It has still to be elucidated whether the decreased pain thresholds in migraine subjects are due to the hereditary liability of a subject for migraine or whether this occurs during the history of migraine as a result of repetitive migraine attack perception.
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We designed allele-specific primers to amplify genomic DNA of patients with Charcot-Marie-Tooth 1A (CMT1andand hereditary neuropathy with liability to pressure palsies (HNPP).
In addition, duplication and deletion of PMP22 are associated with Charcot Marie Tooth disease Type 1A (CMT1andand Hereditary Neuropathy with Liability to Pressure Palsy (HNPP), respectively.
The prevalence of hereditary neuropathy with liability to pressure palsies (HNPP) is estimated to be at least 16 per 100,000 [2100,000
The reciprocal product, a microdeletion, causes hereditary neuropathy with liability to pressure palsies (HNPP) [ 5].
Interestingly, the reduced gene dosage of PMP22 is the most common genetic cause of hereditary neuropathy with liability to pressure palsies (HNPP).
Structural abnormalities of the node may underlie the changes in the excitability in motor axons of patients with hereditary neuropathy with liability to pressure palsies (Jankelowitz and Burke, 2013).
A prominent neuropathological feature of several inherited neuropathies, including hereditary neuropathy with liability to pressure palsies (HNPP) and Charcot-Marie-Tooth disease type 4B1 (CMT4B1) are 'tomacula' or other forms of focally folded myelin.
Five subtypes of CMT (CMT1A/ PMP22 duplication, CMT1X/ GJB1 mutation, CMT2A/ mutationation, CMT1B/ MPZ mutation, and hereditary neuropathy with liability to pressure palsy/ PMP22 deletion) accounted for 89.2% of all genetically confirmed mutations.
This deletion causes the neurological disorder hereditary neuropathy with liability to pressure palsies and was implicated in schizophrenia on the basis of only eight observations in the original case group.
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