Dominant autosomal muscular dystrophy with early contractures and cardiomyopathy (Hauptmann-Thannhauser)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00282089.pdf
Reference6 articles.
1. Becker PE (1972) Neues zur Genetik und Klassifikation der Muskeldystrophien. Humangenetik 17:1
2. Chakrabarti A, Pearce JMS (1981) Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features. J Neurol Neurosurg Psychiatry 44:1146
3. Fenichel GM, Chul Sul Yi, Kilroy AW, Blouin R (1982) An autosomal dominant dystrophy with humeropelvic distribution and cardiomyopathy. Neurology (NY) 32:1399
4. Hauptmann A, Thannhauser SJ (1941) Muscular shortening and dystrophy. A heredofamilial disease. Arch Neurol Psychiatry 46:654
5. Miller RG, Layzer RB, Mellenthin MA, Golabi M, Francoz RA, Mall JC (1985) Emery-Dreifuss muscular dystrophy with autosomal dominant transmission. Neurology (NY) 35:1230
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