Opening book details…
About this book
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability by Elisabeth M. Lodder & Pasquelena De Nittis & Charlotte D. Koopman & Wojciech Wiszniewski & Carolina Fischinger Moura de Souza & Najim Lahrouchi & Nicolas Guex & Valerio Napolioni & Federico Tessadori & Leander Beekman & Eline A. Nannenberg & Lamiae... is a book available to read on EtoBox.
- Author
- Elisabeth M. Lodder & Pasquelena De Nittis & Charlotte D. Koopman & Wojciech Wiszniewski & Carolina Fischinger Moura de Souza & Najim Lahrouchi & Nicolas Guex & Valerio Napolioni & Federico Tessadori & Leander Beekman & Eline A. Nannenberg & Lamiae...
- Publisher
- American Society of Human Genetics
- Language
- EN
More by Elisabeth M. Lodder & Pasquelena De Nittis & Charlotte D. Koopman & Wojciech Wiszniewski & Carolina Fischinger Moura de Souza & Najim Lahrouchi & Nicolas Guex & Valerio Napolioni & Federico Tessadori & Leander Beekman & Eline A. Nannenberg & Lamiae...
Similar books
- Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome — Fuxi Zhu & Fengsong Wang & Xiaoyu Yang & Jingjing Zhang & Huan Wu & Zhou Zhang & Zhiguo Zhang & Xiaojin He & Ping Zhou & Zhaolian Wei & Jozef Gecz & Yunxia Cao
- Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa — Gavin Arno & Smriti A. Agrawal & Aiden Eblimit & James Bellingham & Mingchu Xu & Feng Wang & Christina Chakarova & David A. Parfitt & Amelia Lane & Thomas Burgoyne & Sarah Hull & Keren J. Carss & Alessia Fiorentino & Matthew J. Hayes & Peter M. Munro &... (2016)
- Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome — Anna C. Thomas & Hywel Williams & Núria Setó-Salvia & Chiara Bacchelli & Dagan Jenkins & Mary O’Sullivan & Konstantinos Mengrelis & Miho Ishida & Louise Ocaka & Estelle Chanudet & Chela James & Francesco Lescai & Glenn Anderson & Deborah Morrogh & Mina... (2015)
- Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia — Ziv Gan-Or & Naima Bouslam & Nazha Birouk & Alexandra Lissouba & Daniel B. Chambers & Julie Vérièpe & Alaura Androschuk & Sandra B. Laurent & Daniel Rochefort & Dan Spiegelman & Alexandre Dionne-Laporte & Anna Szuto & Meijiang Liao & Denise A....
- Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta — Shahida Moosa & Guilherme L. Yamamoto & Lutz Garbes & Katharina Keupp & Ana Beleza-Meireles & Carolina Araujo Moreno & Eugenia Ribeiro Valadares & Sérgio B. de Sousa & Sofia Maia & Jorge Saraiva & Rachel S. Honjo & Chong Ae Kim & Hamilton Cabral de... (2019)
- Homozygous SLC6A17 Mutations Cause Autosomal-Recessive Intellectual Disability with Progressive Tremor, Speech Impairment, and Behavioral Problems — Zafar Iqbal & Marjolein H. Willemsen & Marie-Amélie Papon & Luciana Musante & Marco Benevento & Hao Hu & Hanka Venselaar & Willemijn M. Wissink-Lindhout & Anneke T. Vulto-van Silfhout & Lisenka E.L.M. Vissers & Arjan P.M. de Brouwer & Sylviane...