Transient receptor potential genes and human inherited disease

Advances in Experimental Medicine and Biology

Volumn 704, Issue , 2011, Pages 1011-1032

  Everett, Kate V ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

Inherited human disease; Mutations; TRP genes

Indexed keywords

MUCOLIPIN; TRANSCRIPTION FACTOR SOX9; TRANSIENT RECEPTOR POTENTIAL CHANNEL; TRANSIENT RECEPTOR POTENTIAL CHANNEL M; UNCLASSIFIED DRUG; VANILLOID RECEPTOR 1;

AMINO TERMINAL SEQUENCE; BRACHYOLMIA; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CONFERENCE PAPER; CONGENITAL STATIONARY NIGHT BLINDNESS; DISEASE COURSE; DYSPLASIA; FAMILIAL DISEASE; FEEDBACK SYSTEM; FOCAL GLOMERULOSCLEROSIS; GENE; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC DISORDER; HEART BLOCK; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HYPOCALCEMIA; HYPOMAGNESEMIA; KIDNEY POLYCYSTIC DISEASE; METATROPIC DYSPLASIA; MISSENSE MUTATION; MUCOLIPIDOSIS; NEUROMUSCULAR DISEASE; NIGHT BLINDNESS; NONHUMAN; PATHOGENESIS; PATHOPHYSIOLOGY; PKD2 GENE; PRIORITY JOURNAL; PROGRESSIVE FAMILIAL HEART BLOCK; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; SPINAL MUSCULAR ATROPHY; SPONDYLOMETAPHYSEAL DYSPLASIA; TRANSIENT RECEPTOR POTENTIAL GENE; TRPC6 GENE; TRPM1 GENE; TRPM4 GENE; TRPM6 GENE; TRPML1 GENE; TRPP! GENE; TRPV4 GENE; GENETIC PREDISPOSITION; GENETICS; REVIEW;

GENETIC PREDISPOSITION TO DISEASE; HUMANS; TRANSIENT RECEPTOR POTENTIAL CHANNELS;

EID: 79959804266     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-94-007-0265-3_52     Document Type: Conference Paper

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