Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 226,341,793 papers from all fields of science
Search
Sign In
Create Free Account
CAMTA1 wt Allele
Known as:
RP3-467L1.1
, CANPMR
, KIAA0833
Expand
Human CAMTA1 wild-type allele is located within 1p36.31-p36.23 and is approximately 984 kb in length. This allele, which encodes calmodulin-binding…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
3 relations
Broader (1)
CAMTA1 gene
Epithelioid hemangioendothelioma
Transcriptional Regulation
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes
E. Coci
,
U. Koehler
,
+4 authors
J. Riedel
Molecular Cytogenetics
2016
Corpus ID: 15361270
BackgroundNon-progressive cerebellar ataxia with mental retardation (CANPMR, OMIM 614756) and chromosome 1p32-p31 deletion…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE