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Search Results for -
USH1A, FORMERLY
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Also searched for:
RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESS
US1
USH1
USH1A
USH1B
USHER SYNDROME TYPE 1
USHER SYNDROME, TYPE I
USHER SYNDROME, TYPE IA
369 results -
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Repository:
NIGMS Human Genetic Cell Repository
(369)
Collection:
Heritable Diseases
(345)
Retinitis Pigmentosa Foundation Collection
(57)
Apparently Healthy Collection
(19)
Chromosome Abnormalities
(11)
GeT-RM Samples
(8)
PIGI Consented Sample
(6)
dbGaP
(4)
CMD Specific
(2)
Lysosomal Storage Diseases
(2)
Muscular Dystrophies
(2)
Engineered Cell Cultures
(1)
Hereditary Cancers
(1)
Product:
LCL
(181)
DNA
(113)
Fibroblast
(74)
iPSC
(1)
Affected:
Yes
(199)
No
(138)
Mutation Data Available:
N
(258)
Y
(111)
Source:
B-Lymphocyte
(181)
LCL
(91)
Fibroblast
(21)
Skin, Arm
(10)
Skin, Unspecified
(5)
Skin, Skin
(3)
T-Lymphocyte
(2)
Gonad, Gonad
(1)
Skin, Buttock
(1)
Umbilical Cord, Umbilical cord
(1)
Sex:
Female
(194)
Male
(175)
Race:
White
(337)
Black/African American
(9)
Asian
(2)
dbGap Data Available:
No
(369)
Extended Clinical Data Available:
No
(369)
Age at Sampling (Years):
15-24
(71)
25-34
(66)
45-54
(45)
35-44
(44)
5-14
(44)
0-4
(31)
65-74
(25)
55-64
(24)
75-89
(10)
90-99
(1)
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