✦ LIBER ✦

A loss-of-function mutation inCalmodulin2gene affects pollen germination inArabidopsis thaliana

✍ Scribed by Michela Landoni; Alessandra De Francesco; Massimo Galbiati; Chiara Tonelli

Book ID: 106498556
Publisher: Springer
Year: 2010
Tongue: English
Weight: 968 KB
Volume: 74
Category: Article
ISSN: 0167-4412
DOI: 10.1007/s11103-010-9669-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A loss of function mutation in the COL9A

A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome

✍ Stuart Baker; Carol Booth; Corrine Fillman; Michael Shapiro; Michael P. Blair; J 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 561 KB

Late-onset episodic ataxia type 2 associ

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene

✍ Ester Cuenca-León; Isabel Banchs; Selma A. Serra; Pilar Latorre; Noèlia Fernànde 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 732 KB

Loss-of-function mutations of the K+ cha

Loss-of-function mutations of the K+ channel gene KCNJ2 constitute a rare cause of long QT syndrome

✍ Heidi Fodstad; Heikki Swan; Muriel Auberson; Ivan Gautschi; Johannes Loffing; La 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 572 KB

A loss-of-function polymorphic mutation

A loss-of-function polymorphic mutation in the cytolytic P2X7 receptor gene and chronic lymphocytic leukaemia: a molecular study

✍ James S Wiley; L Phuong Dao-Ung; Ben J Gu; Ronald Sluyter; Anne N Shemon; Changp 📂 Article 📅 2002 🏛 The Lancet 🌐 English ⚖ 560 KB

Autosomal Recessive Disorder Otospondylo

Autosomal Recessive Disorder Otospondylomegaepiphyseal Dysplasia Is Associated with Loss-of-Function Mutations in the COL11A2 Gene

✍ Miia Melkoniemi; Han G. Brunner; Sylvie Manouvrier; Raoul Hennekam; Andrea Super 📂 Article 📅 2000 🏛 American Society of Human Genetics 🌐 English ⚖ 571 KB

Loss-of-Function Mutations in the PRPS1

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

✍ Xuezhong Liu; Dongyi Han; Jianzhong Li; Bing Han; Xiaomei Ouyang; Jing Cheng; Xu 📂 Article 📅 2010 🏛 American Society of Human Genetics 🌐 English ⚖ 1014 KB