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A deletion in the myostatin gene causes the compact (Cmpt) hypermuscular mutation in mice

✍ Scribed by Gyula Szabó; Géza Dallmann; Géza Müller; László Patthy; Morris Soller; László Varga

Book ID
106016239
Publisher
Springer-Verlag
Year
1998
Tongue
English
Weight
44 KB
Volume
9
Category
Article
ISSN
0938-8990

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✍ Israela Lerer; Ayala Laufer-Cahana; Jacob R. Rivlin; Arie Augarten; Dvorah Abeli 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 80 KB

A deletion mutation of 8.6Kb in the CFTR gene, spanning the exons 17a, 17b and 18 was identified in 4 homozygous unrelated Palestinian CF patients. The patients were of various ethnic subgroups including Muslims, Christians and Druze. The deletion breakpoint occurred within an identical 4bp sequence