Erratum to: Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases


This study was supported by a research grant from King Salman Center for Disability
Research (FSA) as well as the Saudi Human Genome Project initiative, KACST.Saudi Mendeliome
Group (alphabetical order): Abdulwahab, Firdous; Abouelhoda, Mohamed; Abouthuraya,
Rula; Abumansour, Iman; Ahmed, Syed O.; Al Rubeaan, Khalid; Al Tassan, Nada; AlAbdulaziz,
Basma; AlAbdulrahman, Khalid; Alamer, FH; Alazami, Anas; Al-Baik, Lina A.; Aldahmesh,
Mohammed; Al-Dhekri, Hasan; AlDusery, Haya; Algazlan, Sulaiman; Al-Ghonaium, Abdulaziz;
Alhamed, Mohammed; Alhashem, Amal; Alhissi, Safa Ahmed; AlIssa, Abdulelah; Aljurf,
Mahmoud D.; Alkuraya, Fowzan S; Alkuraya, Hisham; Allam, Rabab; Almasharawi, Iman
J; Almoisheer, Agaadir; AlMostafa, Abeer; Al-Mousa, Hamoud; Al-Muhsen, Saleh; Almutairy,
Eid A; Alnader, Noukha; AlNaqeb, Dhekra; ALOtaibi, AB; Alotibi, Afaf; Al-Qattan, Sarah;
Al-Saud, Bandar; Al-Saud, Haya; Alshammari, M; Alsharif, Hadeel; Alsheikh, Abdulmoneem
H; Al-Sulaiman, Ayman; Altamimi, AS; Al-Tayeb, Hamsa; Alwadaee, SM; Al-Younes, B;
Alzahrani, Fatima; Anazi, Shamsa; Arnaout, Rand; Bashiri, Fahad; Binamer, Yousef;
Binhumaid, FS; Bohlega, Saeed; Broering, Dieter; Burdelski, Martin; Dasouki, Majed
Jamil; Dzimiri, Nduna Francis; Elamin, Tanziel; El-Kalioby, Mohamed; Elsiesy, Hussien;
Faqeih, Eissa; Faquih, Tariq; Hagos, Samya; Hagr, Abdulrahman A; Hashem, Mais; Hawwari,
Abbas; Hazzaa, Selwa; Ibrahim, Niema; Imtiaz, Faiqa; Jabr, Amal; Kattan, Rana; Kaya,
Namik; Kentab, Amal; Khalil, Dania; Khan, Arif O; Khier, Omnia; Meyer, Brian; Mohamed,
Jawahir; Monies, Dorota; Muiya, Paul N.; Murad, Hatem; Naim, EA; Owaidah, Tarek; Patel,
Nisha; Ramzan, Khushnooda; Salih, Mustafa A; Shagrani, Mohammad; Shaheen, Ranad; Shamseldin,
Hanan; Sogaty, Sameera; Subhani, Shazia; Taibah, Khalid; Wakil, Salma M.