Pages that link to "Q36267447"

The following pages link to Disease mechanisms in hereditary sensory and autonomic neuropathies (Q36267447):

Displaying 12 items.

• Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I (Q24301846) (← links)
• Rab and Arf proteins in genetic diseases (Q26862704) (← links)
• Genetic analysis of an allergic rhinitis cohort reveals an intercellular epistasis between FAM134B and CD39. (Q33889692) (← links)
• A short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis (Q33943860) (← links)
• Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene (Q34730628) (← links)
• Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. (Q34995414) (← links)
• Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception (Q36214268) (← links)
• From genes to pain: nerve growth factor and hereditary sensory and autonomic neuropathy type V. (Q38185070) (← links)
• Charcot Marie Tooth 2B Peripheral Sensory Neuropathy: How Rab7 Mutations Impact NGF Signaling? (Q39122072) (← links)
• Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population (Q51574823) (← links)
• Beyond neuropathy in hereditary sensory and autonomic neuropathy type V: cognitive evaluation (Q51890503) (← links)
• Unraveling the Role of Heme in Neurodegeneration (Q57816866) (← links)