Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome
Titel:
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome
Auteur:
Liburd, Nikki Ghosh, Manju Riazuddin, Saima Naz, Sadaf Khan, Shaheen Ahmed, Zubair Riazuddin, Sheikh Liang, Yong Menon, Puthezhath S. Smith, Tenesha Smith, Ann C. Chen, Ken-Shiung Lupski, James R. Wilcox, Edward R. Potocki, Lorraine Friedman, Thomas B.