✦ LIBER ✦

Lavender foal syndrome in Arabian horses is caused by a single-base deletion in the MYO5A gene

✍ Scribed by A. Bierman; A. J. Guthrie; C. K. Harper

Book ID: 114706468
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 151 KB
Volume: 41
Category: Article
ISSN: 0268-9146
DOI: 10.1111/j.1365-2052.2010.02086.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A single base-pair deletion in the WFS1

A single base-pair deletion in the WFS1 gene causes Wolfram syndrome

✍ Pitt, Katherine; James, Chela; Kochar, Inderpal S.; Kapoor, Akshay; Jain, Shilpi 📂 Article 📅 2011 🏛 Walter de Gruyter GmbH & Co. KG 🌐 English ⚖ 144 KB

Neuronal ceroid lipofuscinosis in Devon

Neuronal ceroid lipofuscinosis in Devon cattle is caused by a single base duplication (c.662dupG) in the bovine CLN5 gene

✍ Peter J. Houweling; Julie A.L. Cavanagh; David N. Palmer; Tony Frugier; Nadia L. 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 826 KB

A disease causing deletion of 29 base pa

A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome

✍ B Auber; P Burfeind; S Herold; K Schoner; G Simson; R Rauskolb; H Rehder 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 241 KB

Photosensitive Smith–Lemli–Opitz syndrom

Photosensitive Smith–Lemli–Opitz syndrome is not caused by a single gene mutation: analysis of the gene encoding 7-dehydrocholesterol reductase in five U.K. families

✍ A.V. Anstey; R.M. Azurdia; L.E. Rhodes; A.D. Pearse; P.E. Bowden 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 200 KB

Preferential pre-mRNA utilisation of an

Preferential pre-mRNA utilisation of an upstream cryptic 5′ splice site created by a single base deletion mutation in exon 37 of the FBN-1 gene

✍ Mark A. Gibson; Sarah L. Ellis; Lesley C. Ades; Eric Haan; Edward G. Cleary 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 449 KB

A single base mutation in the 5′ splice

A single base mutation in the 5′ splice site of intron 7 of the lck gene is responsible for the deletion of exon 7 in lck mRNA of the JCaM1 cell line

✍ Rouer, Evelyne; Brule, Fabienne; Benarous, Richard 📂 Article 📅 1999 🏛 Nature Publishing Group 🌐 English ⚖ 615 KB