Phenotypic variability in two brothers with sarcotubular myopathy [3]

Journal of Neurology

Volumn 246, Issue 5, 1999, Pages 408-411

  Muller Felber, W ^a   Schlotter, B ^a   Topfer, M ^a   Ketelsen, U P ^a   Muller Hocker, J ^a   Pongratz, D ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE;

ADULT; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CELL VACUOLE; CREATINE KINASE BLOOD LEVEL; DISEASE COURSE; ECHOGRAPHY; ELECTROMYOGRAPHY; ELECTRON MICROSCOPY; GENETIC VARIABILITY; HISTOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LETTER; MALE; MICROSCOPY; MUSCLE ACTION POTENTIAL; MUSCLE BIOPSY; MYOPATHY; NEUROLOGIC EXAMINATION; PHENOTYPE; PRIORITY JOURNAL; SARCOPLASMIC RETICULUM; TRANSVERSE TUBULAR SYSTEM;

EID: 0033022350     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050374     Document Type: Letter

References (5)