PubMed (OMIM) for id: 374177

Year	Number of Results
1957	1
1962	1
1966	1
1968	2
1973	1
1977	1
1987	1
1989	1
1990	1
1992	1
1993	1
1994	2
1997	1
2000	1
2023	0

1

A sex-linked recessive form of spastic paraplegia.

JOHNSTON AW, McKUSICK VA. JOHNSTON AW, et al. Am J Hum Genet. 1962 Mar;14(1):83-94. Am J Hum Genet. 1962. PMID: 14452137 Free PMC article. No abstract available.

2

Hereditary cerebral palsy; a preliminary report.

BLUMEL J, EVANS EB, EGGERS GW. BLUMEL J, et al. J Pediatr. 1957 Apr;50(4):454-8. doi: 10.1016/s0022-3476(57)80255-8. J Pediatr. 1957. PMID: 13406703 No abstract available.

3

Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease.

Cailloux F, Gauthier-Barichard F, Mimault C, Isabelle V, Courtois V, Giraud G, Dastugue B, Boespflug-Tanguy O. Cailloux F, et al. Eur J Hum Genet. 2000 Nov;8(11):837-45. doi: 10.1038/sj.ejhg.5200537. Eur J Hum Genet. 2000. PMID: 11093273

4

A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.

Naidu S, Dlouhy SR, Geraghty MT, Hodes ME. Naidu S, et al. J Inherit Metab Dis. 1997 Nov;20(6):811-6. doi: 10.1023/a:1005328019832. J Inherit Metab Dis. 1997. PMID: 9427151

5

X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.

Bonneau D, Rozet JM, Bulteau C, Berthier M, Mettey R, Gil R, Munnich A, Le Merrer M. Bonneau D, et al. J Med Genet. 1993 May;30(5):381-4. doi: 10.1136/jmg.30.5.381. J Med Genet. 1993. PMID: 8320699 Free PMC article.

6

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.

Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O. Saugier-Veber P, et al. Nat Genet. 1994 Mar;6(3):257-62. doi: 10.1038/ng0394-257. Nat Genet. 1994. PMID: 8012387

7

The rumpshaker mutation in spastic paraplegia.

Kobayashi H, Hoffman EP, Marks HG. Kobayashi H, et al. Nat Genet. 1994 Jul;7(3):351-2. doi: 10.1038/ng0794-351. Nat Genet. 1994. PMID: 7522741 No abstract available.

8

Sex-linked spastic paraplegia.

Baar HS, Gabriel AM. Baar HS, et al. Am J Ment Defic. 1966 Jul;71(1):13-8. Am J Ment Defic. 1966. PMID: 5964018 No abstract available.

9

Hyperdibasicaminoaciduria: an inherited disorder of amino acid transport.

Whelan DT, Scriver CR. Whelan DT, et al. Pediatr Res. 1968 Nov;2(6):525-34. doi: 10.1203/00006450-196811000-00011. Pediatr Res. 1968. PMID: 5727921 No abstract available.

10

Hind-leg paralysis: a new sex-linked mutation in the Syrian hamster.

Nixon CW, Connelly ME. Nixon CW, et al. J Hered. 1968 Sep-Oct;59(5):276-8. doi: 10.1093/oxfordjournals.jhered.a107718. J Hered. 1968. PMID: 5713627 No abstract available.

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