SMA is a rare genetic disorder causing motor neuron loss and muscle wasting. Caused by SMN1 gene mutation on chromosome 5q. Disease affects voluntary muscles, especially arms, legs and respiratory system. Inherited in autosomal recessive pattern, 2-4% cases occur de novo
NSA uses existing 4G infrastructure with new RAN, while SA requires new 5G core. NSA operates alongside 4G/LTE, SA includes new radio and 5G Core. SA enables end-to-end high-speed with Service-Based Architecture
SMA and RP-SMA are most common FPV connectors developed in 1960s. SMA allows 500+ mating cycles, RP-SMA reverses gender. SMA has pin in center, RP-SMA has hole in center. SMA to RP-SMA conversion is impossible, use adapters instead. Adapters have 0.1-1dB performance loss depending on angle
m-center is u-blox's cellular module evaluation tool. Supports only English language on Windows 10/11 64-bit. Allows connection and testing of cellular modules and evaluation kits
SMA is a genetic disease causing muscle weakness and nerve cell loss. Caused by SMN1 gene defect leading to protein deficiency. Affects approximately 1 in 10,000 newborns
SMA is an inherited neuromuscular disorder causing progressive muscle weakness. Disease affects voluntary movements and is second most common autosomal recessive disorder. SMN1 gene mutation leads to loss of α motor neurons in spinal cord. SMN2 gene copy number determines disease severity, with higher numbers better prognosis