Skoura – a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene
Suriu, C, Khayat, M, Weiler, M, Kfir, N, Cohen, C, Zinger, A, Aslanidis, C, Schmitz, G and Falik‐Zaccai, TC (2009) Skoura – a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene. Clinical Genetics 75 (3), pp. 230-236.Date of publication of this fulltext: 19 Dec 2024 12:10
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| Item type | Article | ||||
| Journal or Publication Title | Clinical Genetics | ||||
| Publisher: | WILEY | ||||
|---|---|---|---|---|---|
| Place of Publication: | HOBOKEN | ||||
| Volume: | 75 | ||||
| Number of Issue or Book Chapter: | 3 | ||||
| Page Range: | pp. 230-236 | ||||
| Date | 2009 | ||||
| Institutions | Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin | ||||
| Identification Number |
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| Keywords | NERVE GROWTH-FACTOR; NEUROPATHY TYPE-IV; RECEPTOR TYROSINE KINASE; CIPA; MANIFESTATIONS; INNERVATION; INVOLVEMENT; MECHANISMS; FRAMESHIFT; ANHYDROSIS; CIPA; hereditary sensory and autonomic neuropathy type IV; MJ; NGF; NTRK1 mutation | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 67346 |
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