Results 191 to 200 of about 16,571 (204)
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A novel RAB7 mutation associated with ulcero‐mutilating neuropathy

Annals of Neurology, 2004
AbstractThere are two known autosomal dominant genes for the hereditary ulcero‐mutilating neuropathies: SPTLC1 (hereditary sensory neuropathy type 1) and RAB7 (Charcot–Marie–Tooth disease type 2B). We report a family with autosomal dominant ulcero‐mutilating neuropathy, developing in the teens and characterized by ulcers, amputations, sensory ...
Henry, Houlden   +6 more
openaire   +2 more sources

Rab‐interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes

EMBO Journal, 2001
Cecilia Bucci   +2 more
exaly  

Dissection of Rab7 localization on phagosome

Biochemical and Biophysical Research Communications, 2009
Sohkichi Matsumoto   +2 more
exaly  

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