Our son ... the scna1 genetic mutationcausesdravet syndrome
genetic mutation during fetal development but(passive) is caused byApert Syndrome
seizures in zebrafish ... the same genetic mutationcausesDravet syndrome
a mutation in genetics(passive) Usually caused byDravet syndrome
the Ser252Phe mutationcausesApert syndrome
sperm ... the mutationcausesApert syndrome
a genetic mutation called SCN1A. Gavin and Owen(passive) is often caused byDravet Syndrome
a genetic mutation identical to the sodium channel gene mutationcausesDravet syndrome
a SCN1A gene mutation(passive) can also be caused byDravet Syndrome
other children ... the SCN1A mutationcausesDravet syndrome
a single mutation in the SCN1A genecausesDravet Syndrome
defective gene mutation(passive) is caused byApert syndrome
a Pro250Arg mutation in FGFR3(passive) is caused byMuenke syndrome
the analogous mutation in humans(passive) caused byApert syndrome
missense mutation ofSCN2AcausingDravet syndrome
a specific gene mutation in the FGFR3 gene(passive) is caused byMuenke syndrome
a change ( mutation ) in the FGFR2 gene(passive) is caused byApert syndrome
a rare mutation on a single gene(passive) is caused byApert syndrome
a mutation in the FGFR3 gene ( P250R(passive) is caused byMuenke syndrome
a mutation in the SCN1A and SCN2A genes(passive) to be caused byDravet syndrome
a mutation in the neuronal sodium channel gene(passive) is caused byDravet syndrome
a singular mutation in one particular gene(passive) is caused byApert syndrome
a mutation of the FGFR2 gene , which influences bone growth(passive) is caused byApert syndrome
a specific genetic mutation in a gene called the fibroblast growth factor receptor type 3 gene ( or FGFR3 gene for short(passive) is caused byMuenke syndrome
a novel splice - site mutation in ABHD5(passive) caused byDorfman syndrome
a P250R mutation in FGFR3 ( OMIM 134934(passive) is caused byMuenke syndrome
Medroxyprogesterone ... to helppreventPickwickian Syndrome
a random mutation of the fibroblast growth factor receptor 2 ( FGFR2 ) gene(passive) may be caused byApert syndrome
mostly ... mutations in the SCN1A gene(passive) is caused ... byDravet syndrome
mutation in the FGFR2 gene with associated facial and skeletal dysplasias(passive) caused byApert syndrome
an S252W or P253R mutation in the FGFR2 gene ( OMIM 176943(passive) is caused bypalate.17 Apert syndrome
a change ( mutation ) in a gene that affects how bones form(passive) is caused byApert syndrome
point mutation ( C749 G ) in the FGFR3 gene(passive) caused byMuenke syndrome
a specific mutation in the FGFR3 gene , called the P250R mutation(passive) is caused byMuenke syndrome
either gain - of - function mutation or loss - of - function(passive) can be caused byDravet syndrome
from a pro250Arg mutation in FGFR-3 on chromosome 4p(passive) is causedMuenke syndrome
the FGFR2 S252W or P253R mutation ( 23 , 62(passive) caused byApert syndrome
22029951 Missense mutation of the sodium channel gene SCN2AcausesDravet syndrome
de novo mutations in the SCN1A gene(passive) is caused byDravet syndrome
not all kinds of SCN1A gene mutationscauseDravet syndrome