Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophy.

Archives of neurology

Volumn 69, Issue 6, 2012, Pages 790-791

  Vlam, Lotte ^a   Schelhaas, Helenius J ^a   van Blitterswijk, Marka ^a   van Vught, Paul W J ^a   de Visser, Marianne ^a   van der Kooi, Anneke J ^a   van der Pol, W Ludo ^a   van den Berg, Leonard H ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

TRPV4 PROTEIN, HUMAN; VANILLOID RECEPTOR;

FEMALE; GENETICS; HUMAN; LETTER; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; SPINAL MUSCULAR ATROPHY;

DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUSCULAR ATROPHY, SPINAL; MUTATION; TRPV CATION CHANNELS;

MLCS; MLOWN;

EID: 84865613025     PISSN: None     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2012.148     Document Type: Letter

References (0)