Myophosphorylase deficiency: The course of an unusual congenital myopathy

Neurology

Volumn 37, Issue 2, 1987, Pages 316-318

  Abarbanel, J M ^a   Potashnik, R ^a   Frisher, S ^a   Moses, S W ^a   Osimani, A ^a   Herishanu, Y ^a  

^a BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOGEN; PHOSPHORYLASE;

ADULT; CASE REPORT; CONGENITAL DISORDER; DIAGNOSIS; ELECTROMYOGRAPHY; ELECTRON MICROSCOPY; ENZYME DEFICIENCY; GLYCOGEN STORAGE DISEASE TYPE 5; HISTOLOGY; HUMAN; MUSCLE; MUSCLE BIOPSY; MUSCLE DISEASE; PRIORITY JOURNAL;

HUMANS; MALE; MIDDLE AGED; MUSCLES; MUSCULAR ATROPHY; PHOSPHORYLASES;

EID: 0023117038     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/wnl.37.2.316     Document Type: Article

References (11)

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