Inga Rebecca Heinen

1PUBLICATIONS
3CO-AUTHORS
Neurology and neuromuscular diseases
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Publications (1)

|Mar 14, 2022
Novel homozygous nonsense mutation in the P5'N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling.

Martin Kirschner, Inga Rebecca Heinen, Steffen Koschmieder

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Frequent Collaborators

1 joint publications

Thomas Eggermann

1 joint publications

Ingo Kurth

1 joint publications

Edgar Jost