Gene table: search width pubmed_id = 28540413


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Neurodevelopmental disorder with hypotonia, neuropathy and deafness - (AR)
3.45
28540413
SPTBN4 (19q13)
Spectrin, Beta, Nonerythrocytic, 4
* Myopathy, Congenital, With Neuropathy And Deafness - CMND