Number of items: 1.
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Wiessner, Manuela, Roos, Andreas, Munn, Christopher J, Viswanathan, Ranjith, Whyte, Tamieka, Cox, Dan, Schoser, Benedikt, Sewry, Caroline, Roper, Helen, Phadke, Rahul et al (show 28 more authors) , Bettolo, Chiara Marini, Barresi, Rita, Charlton, Richard, Bonnemann, Carsten G, Neto, Osorio Abath, Reed, Umbertina C, Zanoteli, Edmar, Moreno, Cristiane Araujo Martins, Ertl-Wagner, Birgit, Stucka, Rolf, De Goede, Christian, da Silva, Tamiris Borges, Hathazi, Denisa, Dell'Aica, Margherita, Zahedi, Rene P, Thiele, Simone, Muller, Juliane, Kingston, Helen, Mueller, Susanna, Curtis, Elizabeth, Walter, Maggie C, Strom, Tim M, Straub, Volker, Bushby, Kate, Muntoni, Francesco, Swan, Laura E ORCID: 0000-0002-6312-6263, Lochmuller, Hanns and Senderek, Jan
(2017)
Mutations in INPPSK, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment.
AMERICAN JOURNAL OF HUMAN GENETICS, 100 (3).
523 - 536.
This list was generated on Sun May 3 17:02:32 2020 BST.