A Rare Cause of High Transaminasemia: Autosomal Muscle Dystrophy with Gamma Sarcoglycan-Reference-Cited by-同舟云学术

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A Rare Cause of High Transaminasemia: Autosomal Muscle Dystrophy with Gamma Sarcoglycan

Published:2001-03 Issue:3 Volume:32 Page:327-329
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology and Nutrition
language:en
Short-container-title:Journal of Pediatric Gastroenterology and Nutrition

Author:

Urganci Nafiye,Erkan Tülay,Serdaroğlu Piraye,Özçelik Gül,Doğan Sema,Kayaalp Nimet

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology, and Child Health

Reference22 articles.

1. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

2. Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

3. Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex

4. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

5. β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Serum Muscle Enzymes in Neuromuscular Disease;Neuromuscular Disorders in Clinical Practice;2013-04-26

2. Incidental raised transaminases: a clue to muscle disease;Annals of Tropical Paediatrics;2006-12

3. Elevated Transaminases: Of Liver or Muscle Origin?;Journal of Pediatric Gastroenterology and Nutrition;2002-01

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