lunes, 29 de octubre de 2018

Genome editing - OMIM - NCBI

Genome editing - OMIM - NCBI

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From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.







7.
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12.
POU5F1/EWS FUSION GENE, INCLUDED
Cytogenetic locations: 6p21.33
13.
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE, INCLUDED
Cytogenetic locations: 1pter-p36.13, 22q12.2, 1pter-p36.13, 21q22.11
14.
HEMOPHILIA B(M), INCLUDED
Cytogenetic locations: Xq27.1
15.
APO-DYSTROPHIN 1, INCLUDED
Cytogenetic locations: Xp21.2-p21.1
16.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1, INCLUDED; MC5DM1, INCLUDED
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