Exact(12)
These are: 1) familial ligand-defective apolipoprotein (apo -B (FLDH), 2) fapo -Bl hypercholesterolaemia type 3 (FLDH and 3) autosomal recessive hypercholesterolaemia (ARH).
Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, Yu CE, Jondro PD, Schmidt SD, Wang K, et al. Candidate gene for the chromosome 1 familial Alzheimer's disease locus.
Figure 1 Familial pedigree.
Each participant was asked to select whether his relationship to the first sexual abuse victim was: (1) familial (e.g., biological or step-child, niece/nephew, grandchild); (2) nonfamilial (e.g., child of friend, neighbour, met through workplace); or, (3) stranger (e.g., knew child for less than 24 h).
Systemic treatment included immunosuppressive and/or immunomodulator therapy in 32 patients [14 with BD, 7 JIA, 8 pars planitis, 1 ankylosing spondylitis, 1 Familial Mediterranean Fever (FMF), and 1 Vogt Koyanagi–Harada disease (VKH ], antibiotic therapy in 10 patients (9 with ocular toxoplasmosis and 1 brucellosis), and antiherpes therapy in 3 patients.
There are four categories of CJD: 1) familial (fCJD) has a very low incidence of 1×10−7/year; 2) sporadic (sCJD) has an incidence in the range of 1 2×10−6/year; 3) new variant (nvCJD) caused by the agent of the bovine spongiform encephalopathy (BSE) and discovered in 1996[2]; and 4) iatrogenic (iCJD).
Similar(48)
Mutations of Nav1.1 are associated with several neurological disorders including GEFS+2, EIEE6, ICEGTC, FHM3 (migraine, familial hemiplegic, 3), and FEB3A (febrile seizures, familial, 3A) (Table 2 and Table 10).
He allocates the motives for return into three categories: 1) familial-personal reasons, 2) economic-occupational reasons and 3) social-patriotic reasons [ 13].
Many allocate the motives for return into three categories: 1) familial-personal reasons, 2) economic-occupational reasons and 3) social-patriotic reasons.
N102S, the site of 17 familial mutations (41% of families), is located at the first transmembrane spanning region.
We identified twelve nucleotide changes in 13 sporadic, 5 familial and 2 cases with unknown family history.
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