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MEBO TMAU urine test

MEBO Research
TMAU Urine Test
United States only
PROGRAM IS PERMANENTLY SUSPENDED AS OF 2 MAY 2017

Click here for
REQUISITION FORM
Incomplete applications
will NOT be processed

SEE UPDATES HERE

1
test
$150 plus
shipping costs
2
tests
$250 plus
shipping costs

TWO PAYMENT PLAN OPTION
Send email to maria.delatorre@meboresearch.org to arrange, AFTER filling out Requisition Form, please.

Test analysis performed in batches of 20 or more

DATE: 2 MAY 2017
Currently on : PROGRAM IS TEMPORARILY SUSPENDED

Samples analyzed since June 2012 :
352
Metabolomic Profiling Study
NCT02683876

Start : Aug 2016
Stage 1 : 27 Canadian volunteers to test
Latest click here (26 oct) :
17 samples returned


Note : Stage 1 is Canada only.
Return cut-off date : passed
Analysis can take 6/8 weeks
Analysis start in/before Nov
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Wednesday, April 2, 2014

DNA Test for TMAU in United States and Europe

GENE TEST

Click on icon
for test information


A list of laboratories in Gene Tests for TRIMETHYLAMINURIA describes the type of test and methods used by various laboratories in Germany, Spain and the United States.

http://www.genetests.org/disorders/?disid=14487
  • TYPES:
    1. Molecular
    2. Biochemical.
  • METHOD:
    1. Sequencing, Capillary
    2. Qualitative Biochemical Analysis
    3. Gentyping (Microarray, Beads, etc.)
    4. Deletion / Duplication / Copy Number
      (Array, MLPA, Q-PCR, etc.)


ORPHANET

Click on icon for information

Orphanet provides a list of labs that perform FMO3 gene sequencing, Molecular diagnosis of TMAU, Biochemical diagnosis of TMAU, Diagnosis of TMAU using Nuclear Magnetic Resonance, (NMR spectrometry) and analysis of trimethylamine in urine, in European countries, such as Austria, France, Germany, Spain, and United Kingdom.


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A REGISTERED PATIENT ORGANIZATION OF


ORPHANET
There is no disease so rare
that it does not deserve attention

Orphanet is the reference portal for information on rare diseases and orphan drugs, for all audiences. Orphanet’s aim is to help improve the diagnosis, care and treatment of patients with rare diseases.

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