MARC보기
LDR01709nmm uu200433 4500
001000000333070
00520240805172131
008181129s2018 |||||||||||||||||c||eng d
020 ▼a 9780438036734
035 ▼a (MiAaPQ)AAI10792066
035 ▼a (MiAaPQ)upenngdas:13197
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 574
1001 ▼a Rohacek, Alex M.
24510 ▼a Discovering Novel Hearing Loss Genes: Roles for Esrp1 and Gas2 in Inner Ear Development and Auditory Function.
260 ▼a [S.l.] : ▼b University of Pennsylvania., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 193 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
500 ▼a Includes supplementary digital materials.
500 ▼a Adviser: Douglas J. Epstein.
5021 ▼a Thesis (Ph.D.)--University of Pennsylvania, 2018.
520 ▼a Hearing loss is the most common form of congenital birth defect, affecting an estimated 35 million children worldwide. To date, nearly 100 genes have been identified which contribute to a deafness phenotype in humans, however, many cases remain
590 ▼a School code: 0175.
650 4 ▼a Developmental biology.
650 4 ▼a Molecular biology.
650 4 ▼a Cellular biology.
690 ▼a 0758
690 ▼a 0307
690 ▼a 0379
71020 ▼a University of Pennsylvania. ▼b Cell and Molecular Biology.
7730 ▼t Dissertation Abstracts International ▼g 79-10B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0175
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14997677 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자