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The first mutation in
CNGA2
in two brothers with anosmia
H G Karstensen,
Y Mang
, T Fark, T Hummel,
N Tommerup
Medical Genetics Program
12
Citations (Scopus)
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CNGA2
in two brothers with anosmia'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Congenital anosmia
100%
Cyclic Nucleotide-Gated Cation Channels
19%
Cyclic Nucleotides
15%
Exome
15%
Genes
15%
Magnetic Resonance Imaging
8%
Mutation
28%
Neuroimaging
11%
Olfaction Disorders
72%
Olfactory Bulb
14%
Olfactory Mucosa
16%
Parturition
8%
Prefrontal Cortex
11%
Signal Transduction
9%
Smell
29%