Opening book details…
About this book
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype by Arjan F. Theil & Elena Botta & Anja Raams & Desiree E.C. Smith & Marisa I. Mendes & Giuseppina Caligiuri & Sarah Giachetti & Silvia Bione & Roberta Carriero & Giordano Liberi & Luca Zardoni & Sigrid M.A. Swagemakers & Gajja S. Salomons & Alain Sarasin... is a book available to read on EtoBox.
- Author
- Arjan F. Theil & Elena Botta & Anja Raams & Desiree E.C. Smith & Marisa I. Mendes & Giuseppina Caligiuri & Sarah Giachetti & Silvia Bione & Roberta Carriero & Giordano Liberi & Luca Zardoni & Sigrid M.A. Swagemakers & Gajja S. Salomons & Alain Sarasin...
- Publisher
- ElsevierCompany.
- Published
- 2019
- Language
- EN
More by Arjan F. Theil & Elena Botta & Anja Raams & Desiree E.C. Smith & Marisa I. Mendes & Giuseppina Caligiuri & Sarah Giachetti & Silvia Bione & Roberta Carriero & Giordano Liberi & Luca Zardoni & Sigrid M.A. Swagemakers & Gajja S. Salomons & Alain Sarasin...
Similar books
- Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans — Francesco Vetrini & Lisa C.A. D’Alessandro & Zeynep C. Akdemir & Alicia Braxton & Mahshid S. Azamian & Mohammad K. Eldomery & Kathryn Miller & Chelsea Kois & Virginia Sack & Natasha Shur & Asha Rijhsinghani & Jignesh Chandarana & Yan Ding & Judy...
- Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa — Andrea Angius & Paolo Uva & Insa Buers & Manuela Oppo & Alessandro Puddu & Stefano Onano & Ivana Persico & Angela Loi & Loredana Marcia & Wolfgang Höhne & Gianmauro Cuccuru & Giorgio Fotia & Manila Deiana & Mara Marongiu & Hatice Tuba Atalay & Sibel... (2016)
- Bi-allelic Variants in INTS11 Are Associated with a Complex Neurological Disorder — Burak Tepe & Erica L. Macke & Marcello Niceta & Monika Weisz Hubshman & Oguz Kanca & Laura Schultz-Rogers & Yuri A. Zarate & G. Bradley Schaefer & Jorge Luis Granadillo De Luque & Daniel J. Wegner & Benjamin Cogne & Brigitte Gilbert-Dussardier & Xavier... (2023)
- Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice — Chunyu Liu & Xiaojin He & Wangjie Liu & Shenmin Yang & Lingbo Wang & Weiyu Li & Huan Wu & Shuyan Tang & Xiaoqing Ni & Jiaxiong Wang & Yang Gao & Shixiong Tian & Lin Zhang & Jiangshan Cong & Zhihua Zhang & Qing Tan & Jingjing Zhang & Hong Li & Yading... (2019)
- Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy — Clara D.M. van Karnebeek & Rúben J. Ramos & Xiao-Yan Wen & Maja Tarailo-Graovac & Joseph G. Gleeson & Cristina Skrypnyk & Koroboshka Brand-Arzamendi & Farhad Karbassi & Mahmoud Y. Issa & Robin van der Lee & Britt I. Drögemöller & Janet Koster & Justine... (2019)
- De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype — Vandana Shashi & Loren D.M. Pena & Katherine Kim & Barbara Burton & Maja Hempel & Kelly Schoch & Magdalena Walkiewicz & Heather M. McLaughlin & Megan Cho & Nicholas Stong & Scott E. Hickey & Christine M. Shuss & Michael S. Freemark & Jane S. Bellet &... (2016)