Orphanet: Diagnostik der autosomal rezessiven Neuromyotonie mit axonaler Neuropathie HINT1 Gen
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Diagnosis of autosomal recessive neuromyotonia and axonal neuropathy (HINT1 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/02/2016
  • Phone : 49 (0)7071 565 44 55
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Last update: February 2016

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of genes tested (including panels) (1)

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.