Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient
Hua Wang
◽
Liang Huo
◽
Yajian Wang
◽
Weiwei Sun
◽
Weiyue Gu
2019 ◽
Vol 7
(5)
◽
pp. e634
Emanuela Ponzi
◽
Viola Alesi
◽
Francesca R. Lepri
◽
Silvia Genovese
◽
Sara Loddo
◽
...
Zakir Lazoğlu
◽
Uğur Aksu
◽
Kamuran Kalkan
◽
Oktay Gulcu
◽
Selim Topcu
2014 ◽
Vol 34
(5)
◽
pp. 390-395
◽
Sulman Basit
◽
Omhani Malibari
◽
Alia Mahmood Al Balwi
◽
Firoz Abdusamad
◽
Feras Abu Ismail
2008 ◽
Vol 146A
(22)
◽
pp. 2911-2915
◽
Benedikt Schoser
◽
Dieter Gläser
◽
Josef Müller-Höcker
2018 ◽
Vol 19
(4)
◽
pp. 203-210
◽
Ferdos Nazari
◽
Farnaz Sinaei
◽
Yalda Nilipour
◽
François Petit
◽
Shahram Oveisgharan
◽
...
2003 ◽
Vol 335
(1-2)
◽
pp. 21-26
◽
Jalaluddin Bhuiyan
◽
Ali N. Al Odaib
◽
Pinar T. Ozand
1972 ◽
Vol 34
(8)
◽
pp. 862-864
◽
C G Miller
◽
G A Alleyne
◽
S E Brooks
2000 ◽
Vol 58
(5)
◽
pp. 409-410
◽
SL Wenger
◽
SC McIntire
◽
V Bansal
◽
JA Barranger
◽
J Higgins
◽
...
P.M. Anstee
◽
D. Concas
◽
B. Wu
◽
P. Potter
◽
R. Cox
◽
...
2012 ◽
Vol 21
(1)
◽
pp. 86-89
◽
S.D. Bolton
◽
V.A. Clark
◽
J.E. Norman