Mutation analysis in myophosphorylase deficiency (McArdle's disease)-Reference-Cited by-同舟云学术

Mutation analysis in myophosphorylase deficiency (McArdle's disease)

Published:1998-03 Issue:3 Volume:43 Page:326-331
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Vorgerd Matthias,Kubisch Christian,Burwinkel Barbara,Reichmann Heinz,Mortier Wilhelm,Tettenborn Barbara,Pongratz Dieter,Lindemuth Rainer,Tegenthoff Martin,Malin Jean-Pierre,Kilimann Manfred W.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference23 articles.

1. A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE

2. CHRONIC PROGRESSIVE MYOPATHY WITH MYOGLOBINURIA: DEMONSTRATION OF A GLYCOGENOLYTIC DEFECT IN THE MUSCLE*

3. Nonlysosomal glycogenoses. In, eds. Myology, vol 2. 2nd ed. New York: McGraw-Hill, 1994: 1554-1576.

4. Intron/exon structure of the human gene for the muscle isozyme of glycogen phosphorylase

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