The condition is usually caused by mutations in a gene called SMN1, which contains instructions for how to make a protein called survival motor neuron (SMN) protein.This protein is critical for ...
A two-and-a-half-year-old girl shows no signs of a rare genetic disorder, after becoming the first person to be treated for the motor-neuron condition while in the womb. The child’s mother took ...
A two-and-a-half-year-old girl shows no signs of a rare genetic disorder, after becoming the first person to be treated for the motor-neuron condition while in the womb. The child’s mother took ...
positivity for neuron-surface antibodies, and (3) reasonable exclusion of other disorders. The exclusion criteria were as follows: (1) history of intrinsic thyroid disorder (hypothyroidism, ...
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